Method for identifying nucleic acid molecules associated with angiogenesis

ABSTRACT

A method for the identification of a nucleic acid molecule differentially expressed in an in vitro model of a biological system, comprising the steps of: (1) harvesting cells from the model system at predetermined time points; (2) obtaining total RNA from the cells harvested at each time point; (3) preparing cDNA from the total RNA from each time point to provide a plurality of pools of cDNA; (4) performing a suppression subtractive hybridization (SSH) on the cDNA pools from each time point sequentially so as to progressively amplify cDNAs derived from nucleic acid molecules differentially expressed from one time period to the next.

TECHNICAL FIELD

The present invention relates to novel nucleic acid sequences (“angiogenic genes”) involved in the process of angiogenesis. Each of the angiogenic genes encode a polypeptide that has a role in angiogenesis. In view of the realisation that these genes play a role in angiogenesis, the invention is also concerned with the therapy of pathologies associated with angiogenesis, the screening of drugs for pro- or anti-angiogenic activity, the diagnosis and prognosis of pathologies associated with angiogenesis, and in some cases the use of the nucleic acid sequences to identify and obtain full-length angiogenesis-related genes.

BACKGROUND ART

The formation of new blood vessels from pre-existing vessels, a process termed angiogenesis, is essential for normal growth. Important angiogenic processes include those taking place in embryogenesis, renewal of the endometrium, formation and growth of the corpus luteum of pregnancy, wound healing and in the restoration of tissue structure and function after injury.

The formation of new capillaries requires a coordinated series of events mediated through the expression of multiple genes which may have either pro- or anti-angiogenic activities. The process begins with an angiogenic stimulus to existing vasculature, usually mediated by growth factors such as vascular endothelial growth factor or basic fibroblast growth factor. This is followed by degradation of the extracellular matrix, cell adhesion changes (and disruption), an increase in cell permeability, proliferation of endothelial cells (ECs) and migration of ECs towards the site of blood vessel formation. Subsequent processes include capillary tube or lumen formation, stabilisation and differentiation by the migrating ECs.

In the (normal) healthy adult, angiogenesis is virtually arrested and occurs only when needed. However, a number of pathological situations are characterised by enhanced, uncontrolled angiogenesis. These conditions include cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis and cardiovascular diseases such as atherosclerosis. In other pathologies such as ischaemic limb disease or in coronary artery disease, growing new vessels through the promotion of an expanding vasculature would be of benefit.

A number of in vitro assays have been established which are thought to mimic angiogenesis and these have provided important tools to examine the mechanisms by which the angiogenic process takes place and the genes most likely to be involved.

Lumen formation is a key step in angiogenesis. The presence of vacuoles within ECs undergoing angiogenesis have been reported and their involvement in lumen formation has been postulated (Folkman and Haudenschild, 1980; Gamble et al., 1993). The general mechanism of lumen formation suggested by Folkman and Haudenschild (1980), has been that vacuoles form within the cytoplasm of a number of aligned ECs which are later converted to a tube. The union of adjacent tubes results in the formation of a continuous unicellular capillary lumen. However, little is known about the changes in cell morphology leading to lumen formation or the signals required for ECs to construct this feature.

An in vitro model of angiogenesis has been created from human umbilical vein ECs plated onto a 3 dimensional collagen matrix (Gamble et al., 1993). In the presence of phorbol myristate acetate (PMA) these cells form capillary tubes within 24 hours. With the addition of anti-integrin antibodies, the usually unicellular tubes (thought to reflect an immature, poorly differentiated phenotype) are converted to form a multicellular lumen through the inhibition of cell-matrix interactions and promotion of cell-cell interactions. This model has subsequently allowed the investigation of the morphological events which occur in lumen formation.

For the treatment of diseases associated with angiogenesis, understanding the molecular genetic mechanisms of the process is of paramount importance. The use of the in vitro model described above (Gamble et al., 1993), a model that reflects the critical events that occur during angiogenesis in vivo in a time dependant and broadly synchronous manner, has provided a tool for the identification of the key genes involved.

DISCLOSURE OF THE INVENTION

Total RNA from cells harvested at specific time points from a biological model, in this case the Gamble et al (1993) model for angiogenesis, were used to prepare cDNAs, which were subjected to a novel process incorporating suppression subtractive hybridization (SSH) to identify cDNAs derived from differentially expressed genes.

According to one aspect of the present invention there is provided a method for the identification of a gene differentially expressed in an in vitro model of a biological system, comprising the steps of:

-   -   (1) harvesting cells from the model system at predetermined time         points;     -   (2) obtaining total RNA from the cells harvested at each time         point;     -   (3) preparing cDNA from the total RNA from each time point to         provide a plurality of pools of cDNA;     -   (4) performing a suppression subtractive hybridization (SSH) on         the cDNA pools from each time point sequentially so as to         progressively amplify cDNAs derived from genes differentially         expressed from one time period to the next.

Thus, up-regulation of a gene whose expression subsequently remains up-regulated at the same level will be detected (and the cDNA amplified) only in the first time period where the level cDNA is elevated, as the quantity of cDNA in pools from the subsequent time points will be the same. This reduction in redundancy reduces the possibility that other genes of lower representation in the cell mRNA expression pool will be masked. In a particularly preferred embodiment of the present invention the model system is an in vitro model for angiogenesis (Gamble et al., 1993).

Those cDNAs identified to be differentially expressed in the SSH process were cloned and subjected to microarray analysis, which lead to the identification of a number of genes that are up-regulated in their expression during the angiogenesis process.

According to a further aspect of the present invention there is provided a method for the identification of a gene up-regulated in an in vitro model of a biological system, comprising the steps of:

-   -   (1) harvesting cells from the model system at predetermined time         points;     -   (2) obtaining total RNA from the cells harvested at each time         point;     -   (3) preparing cDNA from the total RNA from each time point to         provide a plurality of pools of cDNA;     -   (4) performing a suppression subtractive hybridization (SSH) on         the cDNA pools from each time point sequentially so as to         progressively amplify cDNAs derived from genes differentially         expressed from one time period to the next.     -   (5) cloning the amplified cDNAs;     -   (6) locating DNA from each clone on a microarray;     -   (7) generating antisense RNA by reverse transcription of total         RNA from cells harvested from the in vitro model at said         predetermined time intervals and labelling the antisense RNA;         and     -   (8) probing the microarray with labelled antisense RNA from 0         hours and each of the other time points separately to identify         clones containing cDNA derived from genes which are up-regulated         at said time points in the in vitro model.

Functional analysis of a subset of these up-regulated angiogenic genes and their effect on endothelial cell function and capillary tube formation is described in detail below.

Accordingly, the present invention provides isolated nucleic acid molecules, which have been shown to be up-regulated in their expression during angiogenesis (see Tables 1 and 2). The isolation of these angiogenic genes has provided novel targets for the treatment of angiogenesis-related disorders.

In a first aspect of the present invention there is provided an isolated nucleic acid molecule as defined by SEQ ID Numbers: 1 to 44.

Following the realisation that these molecules, and those listed in Tables 1 and 2, are up-regulated in their expression during angiogenesis, the invention provides isolated nucleic acid molecules as defined by SEQ ID Numbers: 1 to 44, and laid out in Tables 1 and 2, or fragments thereof, that play a role in an angiogenic process. Such a process may include, but is not restricted to, embryogenesis, menstrual cycle, wound repair, tumour angiogenesis and exercise induced muscle hypertrophy.

In addition, the present invention provides isolated nucleic acid molecules as defined by SEQ ID Numbers: 1 to 44, and laid out in Tables 1 and 2 (hereinafter referred to as “angiogenic genes”, “angiogenic nucleic acid molecules” or “angiogenic polypeptides” for the sake of convenience), or fragments thereof, that play a role in diseases associated with the angiogenic process. Diseases may include, but are not restricted to, cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis, and cardiovascular diseases such as atherosclerosis, ischaemic limb disease and coronary artery disease. Useful fragments may include those which are unique and which do not overlap any previously identified genes, unique fragments which do overlap with a known sequence, and fragments which span alternative splice junctions etc.

The invention also encompasses an isolated nucleic acid molecule that is at least 70% identical to any one of the angiogenic genes of the invention and which plays a role in the angiogenic process.

Such variants will have preferably at least about 85%, and most preferably at least about 95% sequence identity to the angiogenic genes. Any one of the polynucleotide variants described above can encode an amino acid sequence, which contains at least one functional or structural characteristic of the relevant angiogenic gene of the invention.

Sequence identity is typically calculated using the BLAST algorithm, described in Altschul et al (1997) with the BLOSUM62 default matrix.

The invention also encompasses an isolated nucleic acid molecule which hybridizes under stringent conditions with any one of the angiogenic genes of the invention and which plays a role in an angiogenic process.

Hybridization with PCR probes which are capable of detecting polynucleotide sequences, including genomic sequences, may be used to identify nucleic acid sequences which encode the relevant angiogenic gene. The specificity of the probe, whether it is made from a highly specific region, e.g., the 5′ regulatory region, or from a less specific region, e.g., a conserved motif, and the stringency of the hybridization or amplification will determine whether the probe identifies only naturally occurring sequences encoding the angiogenic gene, allelic variants, or related sequences.

Probes may also be used for the detection of related sequences, and should preferably have at least 50% sequence identity to any of the angiogenic gene-encoding sequences of the invention. The hybridization probes of the present invention may be DNA or RNA and may be derived from any one of the angiogenic gene sequences or from genomic sequences including promoters, enhancers, and introns of the angiogenic genes.

Means for producing specific hybridization probes for DNAs encoding any one of the angiogenic genes include the cloning of polynucleotide sequences encoding the relevant angiogenic gene or its derivatives into vectors for the production of mRNA probes. Such vectors are known in the art, and are commercially available. Hybridization probes may be labelled by radionuclides such as ³²P or ³⁵S, or by enzymatic labels, such as alkaline phosphatase coupled to the probe via avidin/biotin coupling systems, or other methods known in the art.

Under stringent conditions, hybridization with ³²P labelled probes will most preferably occur at 42° C. in 750 mM NaCl, 75 mM trisodium citrate, 2% SDS, 50% formamide, 1× Denhart's, 10% (w/v) dextran sulphate and 100 μg/ml denatured salmon sperm DNA. Useful variations on these conditions will be readily apparent to those skilled in the art. The washing steps which follow hybridization most preferably occur at 65° C. in 15 mM NaCl, 1.5 mM trisodium citrate, and 1% SDS. Additional variations on these conditions will be readily apparent to those skilled in the art.

The nucleic acid molecules, or fragments thereof, of the present invention have a nucleotide sequence obtainable from a natural source. They therefore include naturally occurring normal, naturally occurring mutant, naturally occurring polymorphic alleles, differentially spliced transcripts, splice variants etc. Natural sources include animal cells and tissues, body fluids, tissue culture cells etc.

The nucleic acid molecules of the present invention can also be engineered using methods accepted in the art so as to alter the angiogenic gene-encoding sequences for a variety of purposes. These include, but are not limited to, modification of the cloning, processing, and/or expression of the gene product. PCR reassembly of gene fragments and the use of synthetic oligonucleotides allow the engineering of angiogenic gene nucleotide sequences. For example, oligonucleotide-mediated site-directed mutagenesis can introduce mutations that create new restriction sites, alter glycosylation patterns and produce splice variants etc.

As a result of the degeneracy of the genetic code, a number of nucleic acid sequences encoding the angiogenic genes of the invention, some that may have minimal similarity to the nucleic acid sequences of any known and naturally occurring gene, may be produced. Thus, the invention includes each and every possible variation of polynucleotide sequence that could be made by selecting combinations based on possible codon choices. These combinations are made in accordance with the standard triplet genetic code as applied to the polynucleotide sequence of the naturally occurring angiogenic gene, and all such variations are to be considered as being specifically disclosed.

The nucleic acid molecules of this invention are typically DNA molecules, and include cDNA, genomic DNA, synthetic forms, and mixed polymers, both sense and antisense strands, and may be chemically or biochemically modified, or may contain non-natural or derivatised nucleotide bases as will be appreciated by those skilled in the art. Such modifications include labels, methylation, intercalators, alkylators and modified linkages. In some instances it may be advantageous to produce nucleotide sequences encoding an angiogenic gene or its derivatives possessing a substantially different codon usage than that of the naturally occurring gene. For example, codons may be selected to increase the rate of expression of the peptide in a particular prokaryotic or eukaryotic host corresponding with the frequency that the host utilizes particular codons. Other reasons to alter the nucleotide sequence encoding an angiogenic gene or its derivatives without altering the encoded amino acid sequence include the production of RNA transcripts having more desirable properties, such as a greater half-life, than transcripts produced from the naturally occurring sequence.

The invention also encompasses production of the nucleic acid molecules of the invention, entirely by synthetic chemistry. Synthetic sequences may be inserted into expression vectors and cell systems that contain the necessary elements for transcriptional and translational control of the inserted coding sequence in a suitable host. These elements may include regulatory sequences, promoters, 5′ and 3′ untranslated regions and specific. initiation signals (such as an ATG initiation codon and Kozak consensus sequence) which allow more efficient. translation of sequences encoding the angiogenic genes. In cases where the complete coding sequence including its initiation codon and upstream regulatory sequences are inserted into the appropriate expression vector, additional control signals may not be needed. However, in cases where only coding sequence, or a fragment thereof, is inserted, exogenous translational control signals as described above should be provided by the vector. Such signals may be of various origins, both natural and synthetic. The efficiency of expression may be enhanced by the inclusion of enhancers appropriate for the particular host cell system used (Scharf et al., 1994).

The invention also includes nucleic acid molecules that are the complements of the sequences described herein.

The present invention allows for the preparation of purified polypeptides or proteins. In order to do this, host cells may be transfected with a nucleic acid molecule as described above. Typically, said host cells are transfected with an expression vector comprising a nucleic acid molecule according to the invention. A variety of expression vector/host systems may be utilized to contain and express the sequences. These include, but are not limited to, microorganisms such as bacteria transformed with plasmid or cosmid DNA expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with viral expression vectors (e.g., baculovirus); or mouse or other animal or human tissue cell systems. Mammalian cells can also be used to express a protein that is encoded by a specific angiogenic gene of the invention using various expression vectors including plasmid, cosmid and viral systems such as a vaccinia virus expression system. The invention is not limited by the host cell or vector employed.

The nucleic acid molecules, or variants thereof, of the present invention can be stably expressed in cell lines to allow long term production of recombinant proteins in mammalian systems. Sequences encoding any one of the angiogenic genes of the invention can be transformed into cell lines using expression vectors which may contain viral origins of replication and/or endogenous expression elements and a selectable marker gene on the same or on a separate vector. The selectable marker confers resistance to a selective agent, and its presence allows growth and recovery of cells which successfully express the introduced sequences. Resistant clones of stably transformed cells may be propagated using tissue culture techniques appropriate to the cell type.

The protein produced by a transformed cell may be secreted or retained intracellularly depending on the sequence and/or the vector used. As will be understood by those of skill in the art, expression vectors containing polynucleotides which encode a protein may be designed to contain signal sequences which direct secretion of the protein through a prokaryotic or eukaryotic cell membrane.

In addition, a host cell strain may be chosen for its ability to modulate expression of the inserted sequences or to process the expressed protein in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, glycosylation, phosphorylation, and acylation. Post-translational cleavage of a “prepro” form of the protein may also be used to specify protein targeting, folding, and/or activity. Different host cells having specific cellular machinery and characteristic mechanisms for post-translational activities (e.g., CHO or HeLa cells), are available from the American Type Culture Collection (ATCC) and may be chosen to ensure the correct modification and processing of the foreign protein.

According to still another aspect of the present invention there is provided an expression vector comprising a nucleic acid molecule of the invention as described above.

According to still another aspect of the present invention there is provided a cell comprising a nucleic acid molecule of the invention as described above.

When large quantities of protein are needed such as for antibody production, vectors which direct high levels of expression may be used such as those containing the T5 or T7 inducible bacteriophage promoter. The present invention also includes the use of the expression systems described above in generating and isolating fusion proteins which contain important functional domains of the protein. These fusion proteins are used for binding, structural and functional studies as well as for the generation of appropriate antibodies.

In order to express and purify the protein as a fusion protein, the appropriate polynucleotide sequences of the present invention are inserted into a vector which contains a nucleotide sequence encoding another peptide (for example, glutathionine succinyl transferase). The fusion protein is expressed and recovered from prokaryotic or eukaryotic cells. The fusion protein can then be purified by affinity chromatography based upon the fusion vector sequence and the relevant protein can subsequently be obtained by enzymatic cleavage of the fusion protein.

Fragments of polypeptides of the present invention may also be produced by direct peptide synthesis using solid-phase techniques. Automated synthesis may be achieved by using the ABI 431A Peptide Synthesizer (Perkin-Elmer). Various fragments of polypeptide may be synthesized separately and then combined to produce the full length molecule.

In instances where the isolated nucleic acid molecules of the invention represent only partial gene sequence, these partial sequences can be used to obtain the corresponding sequence of the full-length angiogenic gene. Therefore, the present invention further provides the use of a partial nucleic acid molecule of the invention comprising a nucleotide sequence defined by any one of SEQ ID Numbers: 1 to 15, 17 to 37, and 39 to 44 to identify and/or obtain full-length human genes involved in the angiogenic process. Full-length angiogenic genes may be cloned using the partial nucleotide sequences of the invention by methods known per se to those skilled in the art. For example, in silico analysis of sequence databases such as those hosted at the National Centre for Biotechnology Information (http://www.nebi.nlm.nih.gov/) can be searched in order to obtain overlapping nucleotide sequence. This provides a “walking” strategy towards obtaining the full-length gene sequence. Appropriate databases to search at this site include the expressed sequence tag (EST) database (database of GenBank, EMBL and DDBJ sequences from their EST divisions) or the non redundant (nr) database (contains all GenBank, EMBL, DDBJ and PDB sequences but does not include EST, STS, GSS, or phase 0, 1 or 2 HTGS sequences). Typically searches are performed using the BLAST algorithm described in Altschul et al (1997) with the BLOSUM62 default matrix. In instances where in silico “walking” approaches fail to retrieve the complete gene sequence, additional strategies may be employed. These include the use of “restriction-site PCR” will allows the retrieval of unknown sequence adjacent to a portion of DNA whose sequence is known. In this technique universal primers are used to retrieve unknown sequence. Inverse PCR may also be used, in which primers based on the known sequence are designed to amplify adjacent unknown sequences. These upstream sequences may include promoters and regulatory elements. In addition, various other PCR-based techniques may be used, for example a kit available from Clontech (Palo Alto, Calif.) allows for a walking PCR technique, the 5′RACE kit (Gibco-BRL) allows isolation of additional 5′ gene sequence, while additional 3′ sequence can be obtained using practised techniques (for example see Gecz et al., 1997).

In a further aspect of the present invention there is provided an isolated polypeptide as defined by SEQ ID Numbers: 51 to 58 and laid out in Table 1.

The present invention also provides isolated polypeptides, which have been shown to be up-regulated in their expression during angiogenesis (see Tables 1 and 2).

More specifically, following the realisation that these polypeptides are up-regulated in their expression during angiogenesis, the invention provides isolated polypeptides as defined by SEQ ID Numbers: 51 to 58, and as laid out in Tables 1 and 2, or fragments thereof, that play a role in an angiogenic process. Such a process may include, but is not restricted to, embryogenesis, menstrual cycle, wound repair, tumour angiogenesis and exercise induced muscle hypertrophy.

In addition, the present invention provides isolated polypeptides as defined by SEQ ID Numbers: 51 to 58, and as laid out in Tables 1 and 2, or fragments thereof, that play a role in diseases associated with the angiogenic process. Diseases may include, but are not restricted to, cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis, and cardiovascular diseases such as atherosclerosis, ischaemic limb disease and coronary artery disease.

The invention also encompasses an isolated polypeptide having at least 70%, preferably 85%, and more preferably 95%, identity to any one of SEQ ID Numbers: 51 to 58, and which plays a role in an angiogenic process.

Sequence identity is typically calculated using the BLAST algorithm, described in Altschul et al (1997) with the BLOSUM62 default matrix.

In a further aspect of the invention there is provided a method of preparing a polypeptide as described above, comprising the steps of:

(1) culturing cells as described above under conditions effective for production of the polypeptide; and

(2) harvesting the polypeptide.

According to still another aspect of the invention there is provided a polypeptide which is the product of the process described above.

Substantially purified protein or fragments thereof can then be used in further biochemical analyses to establish secondary and tertiary structure. Such methodology is known in the art and includes, but is not restricted to, X-ray crystallography of crystals of the proteins or by nuclear magnetic resonance (NMR). Determination of structure allows for the rational design of pharmaceuticals to interact with the protein, alter protein charge configuration or charge interaction with other proteins, or to alter its function in the cell.

The invention has provided a number of genes likely to be involved in angiogenesis and therefore enables methods for the modulation of angiogenesis. As angiogenesis is critical in a number of pathological processes, the invention therefore also enables therapeutic methods for the treatment of all angiogenesis-related disorders, and may enable the diagnosis or prognosis of all angiogenesis-related disorders associated with abnormalities in expression and/or function of any one of the angiogenic genes.

Examples of such disorders include, but are not limited to, cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis, and cardiovascular diseases such as atherosclerosis, ischaemic limb disease and coronary artery disease.

Therapeutic Applications

According to another aspect of the present invention there is provided a method of treating an angiogenesis-related disorder as described above, comprising administering a selective antagonist or agonist of an angiogenic gene or protein of the invention to a subject in need of such treatment.

In still another aspect of the invention there is provided the use of a selective antagonist or agonist of an angiogenic gene or protein of the invention in the manufacture of a medicament for the treatment of an angiogenesis-related disorder as described above.

For the treatment of angiogenesis-related disorders which result in uncontrolled or enhanced angiogenesis, including but not limited to, cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis and cardiovascular diseases such as atherosclerosis, therapies which inhibit the expanding vasculature are desirable. This would involve inhibition of any one of the angiogenic genes or proteins that are able to promote angiogenesis, or enhancement, stimulation or re-activation of any one of the angiogenic genes or proteins that are able to inhibit angiogenesis.

For the treatment of angiogenesis-related disorders which are characterised by inhibited or decreased angiogenesis, including but not limited to, ischaemic limb disease and coronary artery disease, therapies which enhance or promote vascular expansion are desirable. This would involve inhibition of any one of the angiogenic genes or proteins that are able to restrict angiogenesis or enhancement, stimulation or re-activation of any one of the angiogenic genes or proteins that are able to promote angiogenesis.

For instance, decreasing the expression of BNO782 and BNO481 has been shown to disrupt endothelial cell activity leading to an inhibition of capillary tube formation and angiogenesis. Therefore, in the treatment of disorders where angiogenesis needs to be restricted, it would be desirable to inhibit the function of these genes.

Alternatively, in the treatment of disorders where angiogenesis needs to be stimulated it may be desirable to enhance the function of these genes.

For each of these cases, the relevant therapy will be useful in treating angiogenesis-related disorders regardless of whether there is a lesion in the angiogenic gene.

Inhibiting Gene or Protein Function

Inhibiting the function of a gene or protein can be achieved in a variety of ways. Antisense nucleic acid methodologies represent one approach to inactivate genes that are causative of a disorder. Antisense or gene-targeted silencing strategies may include, but are not limited to, the use of antisense oligonucleotides, injection of antisense RNA, transfection of antisense RNA expression vectors, and the use of RNA interference (RNAi) or short interfering RNAs (siRNA). RNAi can be used in vitro and in vivo to silence a gene when its expression contributes to angiogenesis (Sharp and Zamore, 2000; Grishok et al., 2001). Still further, catalytic nucleic acid molecules such as DNAzymes and ribozymes may be used for gene silencing (Breaker and Joyce, 1994; Haseloff and Gerlach, 1988). These molecules function by cleaving their target mRNA molecule rather than merely binding to it as in traditional antisense approaches.

In one aspect of the invention an isolated nucleic acid molecule, which is the complement of any one of the relevant angiogenic nucleic acid molecules described above may be administered to a subject in need of such treatment. Typically, a complement to any relevant one of the angiogenic genes is administered to a subject to treat or prevent an angiogenesis-related disorder. In a further aspect the complement may encode an RNA molecule that hybridizes with the mRNA encoded by the relevant angiogenic gene of the invention or may be a short interfering oligonucleotide (siRNA) that hybridizes with the mRNA encoded by the relevant angiogenic gene of the invention.

In a further aspect of the invention there is provided the use of an isolated nucleic acid molecule which is the complement of any one of the relevant nucleic acid molecules of the invention and which encodes an RNA molecule or a short interfering oligonucleotide (siRNA) that hybridizes with the mRNA encoded by the relevant angiogenic gene of the invention, in the manufacture of a medicament for the treatment of an angiogenesis-related. disorder.

Typically, a vector expressing the complement of a polynucleotide encoding any one of the relevant angiogenic genes may be administered to a subject to treat or prevent an angiogenesis-related disorder including, but not limited to, those described above. Many methods for introducing vectors into cells or tissues are available and equally suitable for use in vivo, in vitro, and ex vivo. For ex vivo therapy, vectors may be introduced into stem cells taken from the patient and clonally propagated for autologous transplant back into that same patient. Delivery by transfection, by liposome injections, or by polycationic amino polymers may be achieved using methods which are well known in the art. (For example, see Goldman et al., 1997).

In a further aspect purified protein according to the invention may be used to produce antibodies which specifically bind any relevant angiogenic protein of the invention. These antibodies may be used directly as an antagonist or indirectly as a targeting or delivery mechanism for bringing a pharmaceutical agent (such as a cytotoxic agent) to cells or tissues that express the relevant angiogenic protein. Such antibodies may include, but are not limited to, polyclonal, monoclonal, chimeric and single chain antibodies as would be understood by the person skilled in the art.

For the production of antibodies, various hosts including rabbits, rats, goats, mice, humans, and others may be immunized by injection with a protein of the invention or with any fragment or oligopeptide thereof, which has immunogenic properties. Various adjuvants may be used to increase immunological response and include, but are not limited to, Freund's, mineral gels such as aluminum hydroxide, and surface-active substances such as lysolecithin. Adjuvants used in humans include BCG (bacilli Calmette-Guerin) and Corynebacterium parvum.

It is preferred that the oligopeptides, peptides, or fragments used to induce antibodies to the relevant angiogenic protein have an amino acid sequence consisting of at least about 5 amino acids, and, more preferably, of at least about 10 amino acids. It is also preferable that these oligopeptides, peptides, or fragments are identical to a portion of the amino acid sequence of the natural protein and contain the entire amino acid sequence of a small, naturally occurring molecule. Short stretches of amino acids from these proteins may be fused with those of another protein, such as KLH, and antibodies to the chimeric molecule may be produced.

Monoclonal antibodies to any relevant angiogenic protein may be prepared using any technique which provides for the production of antibody molecules by continuous cell lines in culture. These include, but are not limited to, the hybridoma technique, the human B-cell hybridoma technique, and the EBV-hybridoma technique. (For example, see Kohler and Milstein, 1975; Kozbor et al., 1985; Cote et al., 1983; Cole et al., 1984).

Monoclonal antibodies produced may include, but are not limited to, mouse-derived antibodies, humanised antibodies and fully-human antibodies. For example, antibodies are obtained from transgenic mice that have been engineered to produce specific human antibodies in response to antigenic challenge. In one example of this technique, elements of the human heavy and light chain loci are introduced into strains of mice derived from embryonic stem cell lines that contain targeted disruptions of the endogenous heavy and light chain loci. These transgenic mice can synthesise human antibodies specific for human antigens and can be used to produce human antibody-secreting hybridomas. Methods for obtaining human antibodies from transgenic mice are described for example in Lonberg et al., 1994; Green et al., 1994; Taylor et al., 1994.

Antibodies may also be produced by inducing in vivo production in the lymphocyte population or by screening immunoglobulin libraries or panels of highly specific binding reagents as disclosed in the literature. (For example, see Orlandi et al., 1989; Winter et al., 1991).

Antibody fragments which contain specific binding sites for any relevant angiogenic protein may also be generated. For example, such fragments include, F(ab′)2 fragments produced by pepsin digestion of the antibody molecule and Fab fragments generated by reducing the disulfide bridges of the F(ab′)2 fragments. Alternatively, Fab expression libraries may be constructed to allow rapid and easy identification of monoclonal Fab fragments with the desired specificity. (For example, see Huse et al., 1989).

Various immunoassays may be used for screening to identify antibodies having the desired specificity. Numerous protocols for competitive binding or immunoradiometric assays using either polyclonal or monoclonal antibodies with established specificities are well known in the art. Such immunoassays typically involve the measurement of complex formation between a protein and its specific antibody. A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering epitopes is preferred, but a competitive binding assay may also be employed.

In a further aspect, antagonists may include peptides, phosphopeptides or small organic or inorganic compounds. These antagonists should disrupt the function of any relevant angiogenic gene of the invention so as to provide the necessary therapeutic effect.

Peptides, phosphopeptides or small organic or inorganic compounds suitable for therapeutic applications may be identified using nucleic acids and polypeptides of the invention in drug screening applications as described below.

Enhancing Gene or Protein Function

Enhancing, stimulating or re-activating a gene's or protein's function can be achieved in a variety of ways. In one aspect of the invention administration of an isolated nucleic acid molecule, as described above, to a subject in need of such treatment may be initiated. Typically, any relevant angiogenic gene of the invention can be administered to a subject to treat or prevent an angiogenesis-related disorder.

In a further aspect, there is provided the use of an isolated nucleic acid molecule, as described above, in the manufacture of a medicament for the treatment of an angiogenesis-related disorder.

Typically, a vector capable of expressing any relevant angiogenic gene, or a fragment or derivative thereof, may be administered to a subject to treat or prevent a disorder including, but not limited to, those described above. Transducing retroviral vectors are often used for somatic cell gene therapy because of their high efficiency of infection and stable integration and expression. Any relevant full-length gene, or portions thereof, can be cloned into a retroviral vector and expression may be driven from its endogenous promoter or from the retroviral long terminal repeat or from a promoter specific for the target cell type of interest. Other viral vectors can be used and include, as is known in the art, adenoviruses, adeno-associated viruses, vaccinia viruses, papovaviruses, lentiviruses and retroviruses of avian, murine and human origin.

Gene therapy would be carried out according to established methods (Friedman, 1991; Culver, 1996). A vector containing a copy of any relevant angiogenic gene linked to expression control elements and capable of replicating inside the cells is prepared. Alternatively the vector may be replication deficient and may require helper cells for replication and use in gene therapy.

Gene transfer using non-viral methods of infection in. vitro can also be used. These methods include direct injection of DNA, uptake of naked DNA in the presence of calcium phosphate, electroporation, protoplast fusion or liposome delivery. Gene transfer can also be achieved by delivery as a part of a human artificial chromosome or receptor-mediated gene transfer. This involves linking the DNA to a targeting molecule that will bind to specific cell-surface receptors to induce endocytosis and transfer of the DNA into mammalian cells. One such technique uses poly-L-lysine to link asialoglycoprotein to DNA. An adenovirus is also added to the complex to disrupt the lysosomes and thus allow the DNA to avoid degradation and move to the nucleus. Infusion of these particles intravenously has resulted in gene transfer into hepatocytes.

Although not identified to date, it is possible that certain individuals with angiogenesis-related disorders contain an abnormality in any one of the angiogenic genes of the invention. In affected subjects that express a mutated form of any one of the angiogenic genes of the invention it may be possible to prevent the disorder by introducing into the affected cells a wild-type copy of the gene such that it recombines with the mutant gene. This requires a double recombination event for the correction of the gene mutation. Vectors for the introduction of genes in these ways are known in the art, and any suitable vector may be used. Alternatively, introducing another copy of the gene bearing a second mutation in that gene may be employed so as to negate the original gene mutation and block any negative effect.

In a still further aspect, there is provided a method of treating an angiogenesis-related disorder comprising administering a polypeptide, as described above, or an agonist thereof, to a subject in need of such treatment.

In another aspect the invention provides the use of a polypeptide as described above, or an agonist thereof, in the manufacture of a medicament for the treatment of an angiogenesis-related disorder. Examples of such disorders are described above.

In a further aspect, a suitable agonist may also include peptides, phosphopeptides or small organic or inorganic compounds that can mimic the function of any relevant angiogenic gene, or may include an antibody to any relevant angiogenic gene that is able to restore function to a normal level.

Peptides, phosphopeptides or small organic or inorganic compounds suitable for therapeutic applications may be identified using nucleic acids and polypeptides of the invention in drug screening applications as described below.

In further embodiments, any of the agonists, antagonists, complementary sequences, nucleic acid molecules, proteins, antibodies, or vectors of the invention may be administered in combination with other appropriate therapeutic agents. Selection of the appropriate agents may be made by those skilled in the art, according to conventional pharmaceutical principles. The combination of therapeutic agents may act synergistically to effect the treatment or prevention of the various disorders described above. Using this approach, therapeutic efficacy with lower dosages of each agent may be possible, thus reducing the potential for adverse side effects.

Any of the therapeutic methods described above may be applied to any subject in need of such therapy, including, for example, mammals such as dogs, cats, cows, horses, rabbits, monkeys, and most preferably, humans.

Modulation of Angiogenesis

As the invention has provided a number of genes likely to be involved in angiogenesis it therefore enables methods for the modulation of angiogenesis. In a further aspect of the present invention, any of the methods described above used for the treatment of an angiogenesis-related disorder may be used for the modulation of angiogenesis in any system comprising cells. These systems may include but are not limited to, in vitro assay systems (e.g. Matrigel assays, proliferation assays, migration assays, collagen assays, bovine capillary endothelial cell assay etc), in vivo assay systems (e.g. in vivo Matrigel-type assays, chicken chorioallantoic membrane assay, isolated organs, tissues or cells etc), animal models (e.g. in vivo neovascularisation assays, tumour angiogenesis models etc) or hosts in need of treatment (e.g. hosts suffering from angiogenesis-related disorders as previously described.

Drug Screening

According to still another aspect of the invention, nucleic acid molecules of the invention as well as peptides of the invention, particularly any relevant purified angiogenic polypeptides or fragments thereof, and cells expressing these are useful for screening of candidate pharmaceutical compounds in a variety of techniques for the treatment of angiogenesis-related disorders.

Still further, it provides the use wherein high throughput screening techniques are employed.

Compounds that can be screened in accordance with the invention include, but are not limited to peptides (such as soluble peptides), phosphopeptides and small organic or inorganic molecules (such as natural product or synthetic chemical libraries and peptidomimetics).

In one embodiment, a screening assay may include a cell-based assay utilising eukaryotic or prokaryotic host cells that are stably transformed with recombinant nucleic acid molecules expressing the relevant angiogenic polypeptide or fragment, in competitive binding assays. Binding assays will measure for the formation of complexes between the relevant polypeptide or fragments thereof and the compound being tested, or will measure the degree to which a compound being tested will interfere with the formation of a complex between the relevant polypeptide or fragment thereof, and its interactor or ligand.

Non cell-based assays may also be used for identifying compounds that interrupt binding between the polypeptides of the invention and their interactors. Such assays are known in the art and include for example AlphaScreen technology (PerkinElmer Life Sciences, MA, USA). This application relies on the use of beads such that each interaction partner is bound to a separate bead via an antibody. Interaction of each partner will bring the beads into proximity, such that laser excitation initiates a number of chemical reactions ultimately leading to fluorophores emitting a light signal. Candidate compounds that disrupt the binding of the relevant angiogenic polypeptide with its interactor will result in loss of light emission enabling identification and isolation of the responsible compound.

High-throughput drug screening techniques may also employ methods as described in WO84/03564. Small peptide test compounds synthesised on a solid substrate can be assayed through relevant angiogenic polypeptide binding and washing. The relevant bound angiogenic polypeptide is then detected by methods well known in the art. In a variation of this technique, purified angiogenic polypeptides can be coated directly onto plates to identify interacting test compounds.

An additional method for drug screening involves the use of host eukaryotic cell lines that carry mutations in any relevant angiogenic gene of the invention. The host cell lines are also defective at the polypeptide level. Other cell lines may be used where the expression of the relevant angiogenic gene can be regulated (i.e. over-expressed, under-expressed, or switched off). The host cell lines or cells are grown in the presence of various drug compounds and the rate of growth of the host cells is measured to determine if the compound is capable of regulating the growth of defective cells.

The angiogenic polypeptides of the present invention may also be used for screening compounds developed as a result of combinatorial library technology. This provides a way to test a large number of different substances for their ability to modulate activity of a polypeptide. A substance identified as a modulator of polypeptide function may be peptide or non-peptide in nature. Non-peptide “small molecules” are often preferred for many in vivo pharmaceutical applications. In addition, a mimic or mimetic of the substance may be designed for pharmaceutical use. The design of mimetics based on a known pharmaceutically active compound (“lead” compound) is a common approach to the development of novel pharmaceuticals. This is often desirable where the original active compound is difficult or expensive to synthesise or where it provides an unsuitable method of administration. In the design of a mimetic, particular parts of the original active compound that are important in determining the target property are identified. These parts or residues constituting the active region of the compound are known as its pharmacophore. Once found, the pharmacophore structure is modelled according to its physical properties using data from a range of sources including x-ray diffraction data and NMR. A template molecule is then selected onto which chemical groups that mimic the pharmacophore can be added. The selection can be made such that the mimetic is easy to synthesise, is likely to be pharmacologically acceptable, does not degrade in vivo and retains the biological activity of the lead compound. Further optimisation or modification can be carried out to select one or more final mimetics useful for in vivo or clinical testing.

It is also possible to isolate a target-specific antibody and then solve its crystal structure. In principle, this approach yields a pharmacophore upon which subsequent drug design can be based as described above. It may be possible to avoid protein crystallography altogether by generating anti-idiotypic antibodies (anti-ids) to a functional, pharmacologically active antibody. As a mirror image of a mirror image, the binding site of the anti-ids would be expected to be an analogue of the original binding site. The anti-id could then be used to isolate peptides from chemically or biologically produced peptide banks.

Another alternative method for drug screening relies on structure-based rational drug design. Determination of the three dimensional structure of the polypeptides of the invention, or the three dimensional structure of the protein complexes which may incorporate these polypeptides allows for structure-based drug design to identify biologically active lead compounds.

Three dimensional structural models can be generated by a number of applications, some of which include experimental models such as x-ray crystallography and NMR and/or from in silico studies using information from structural databases such as the Protein Databank (PDB). In addition, three dimensional structural models can be determined using a number of known protein structure prediction techniques based on the primary sequences of the polypeptides (e.g. SYBYL—Tripos Associated, St. Louis, Mo.), de novo protein structure design programs (e.g. MODELER—MSI Inc., San Diego, Calif., or MOE—Chemical Computing Group, Montreal, Canada) or ab initio methods (e.g. see U.S. Pat. Nos. 5,331,573 and 5,579,250).

Once the three dimensional structure of a polypeptide or polypeptide complex has been determined, structure-based drug discovery techniques can be employed to design biologically active compounds based on these three dimensional structures. Such techniques are known in the art and include examples such as DOCK (University of California, San Francisco) or AUTODOCK (Scripps Research Institute, La Jolla, Calif.). A computational docking protocol will identify the active site or sites that are deemed important for protein activity based on a predicted protein model. Molecular databases, such as the Available Chemicals Directory (ACD) are then screened for molecules that complement the protein model.

Using methods such as these, potential clinical drug candidates can be identified and computationally ranked in order to reduce the time and expense associated with typical ‘wet lab’ drug screening methodologies.

Compounds identified from the screening methods described above form a part of the present invention, as do pharmaceutical compositions containing these and a pharmaceutically acceptable carrier.

Pharmaceutical Preparations

Compounds identified from screening assays as indicated above can be administered to a patient at a therapeutically effective dose to treat or ameliorate a disorder associated with angiogenesis. A therapeutically effective dose refers to that amount of the compound sufficient to result in amelioration of symptoms of the disorder.

Toxicity and therapeutic efficacy of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals. The data obtained from these studies can then be used in the formulation of a range of dosages for use in humans.

Pharmaceutical compositions for use in accordance with the present invention can be formulated in a conventional manner using one or more physiological acceptable carriers, excipients or stabilisers which are well known. Acceptable carriers, excipients or stabilizers are non-toxic at the dosages and concentrations employed, and include buffers such as phosphate, citrate, and other organic acids; antioxidants including absorbic acid; low, molecular weight (less than about 10 residues) polypeptides; proteins, such as serum albumin, gelatin, or immunoglobulins; binding agents including hydrophilic polymers such as polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagine, arginine or lysine; monosaccharides, disaccharides, and other carbohydrates including glucose, mannose, or dextrins; chelating agents such as EDTA; sugar alcohols such as mannitol or sorbitol; salt-forming counterions such as sodium; and/or non-ionic surfactants such as Tween, Pluronics or polyethylene glycol (PEG).

The formulation of pharmaceutical compositions for use in accordance with the present invention will be based on the proposed route of administration. Routes of administration may include, but are not limited to, inhalation, insufflation (either through the mouth or nose), oral, buccal, rectal or parental administration.

Diagnostic and Prognostic Applications

Should abnormalities in any one of the angiogenic genes of the invention exist, which alter activity and/or expression of the gene to give rise to angiogenesis-related disorders, the polynucleotides and polypeptides of the invention may be used for the diagnosis or prognosis of these disorders, or a predisposition to such disorders. Examples of such disorders include, but are not limited to, cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis, cardiovascular diseases such as atherosclerosis, ischaemic limb disease and coronary artery disease. Diagnosis or prognosis may be used to determine the severity, type or stage of the disease state in order to initiate an appropriate therapeutic intervention.

In another embodiment of the invention, the polynucleotides that may be used for diagnostic or prognostic purposes include oligonucleotide sequences, genomic DNA and complementary RNA and DNA molecules. The polynucleotides may be used to detect and quantitate gene expression in biopsied tissues in which abnormal expression or mutations in any one of the angiogenic genes may be correlated with disease. Genomic DNA used for the diagnosis or prognosis may be obtained from body cells, such as those present in the blood, tissue biopsy, surgical specimen, or autopsy material. The DNA may be isolated and used directly for detection of a specific sequence or may be amplified by the polymerase chain reaction (PCR) prior to analysis. Similarly, RNA or cDNA may also be used, with or without PCR amplification. To detect a specific nucleic acid sequence, direct nucleotide sequencing, reverse transcriptase PCR (RT-PCR), hybridization using specific oligonucleotides, restriction enzyme digest and mapping, PCR mapping, RNAse protection, and various other methods may be employed. oligonucleotides specific to particular sequences can be chemically synthesized and labelled radioactively or nonradioactively and hybridized to individual samples immobilized on membranes or other solid-supports or in solution. The presence, absence or excess expression of any one of the angiogenic genes may then be visualized using methods such as autoradiography, fluorometry, or colorimetry.

In a particular aspect, the nucleotide sequences of the invention may be useful in assays that detect the presence of associated disorders, particularly those mentioned previously. The nucleotide sequences may be labelled by standard methods and added to a fluid or tissue sample from a patient under conditions suitable for the formation of hybridization complexes. After a suitable incubation period, the sample is washed and the signal is quantitated and compared with a standard value. If the amount of signal in the patient sample is significantly altered in comparison to a control sample then the presence of altered levels of nucleotide sequences in the sample indicates the presence of the associated disorder. Such assays may also be used to evaluate the efficacy of a particular therapeutic treatment regimen in animal studies, in clinical trials, or to monitor the treatments of an individual patient.

In order to provide a basis for the diagnosis or prognosis of an angiogenesis-related disorder associated with a mutation in any one of the angiogenic genes of the invention, the nucleotide sequence of the relevant gene can be compared between normal tissue and diseased tissue in order to establish whether the patient expresses a mutant gene.

In order to provide a basis for the diagnosis or prognosis of a disorder associated with abnormal expression of any one of the angiogenic genes of the invention, a normal or standard profile for expression is established. This may be accomplished by combining body fluids or cell extracts taken from normal subjects, either animal or human, with a sequence, or a fragment thereof, encoding the relevant angiogenic gene, under conditions suitable for hybridization or amplification. Standard hybridization may be quantified by comparing the values obtained from normal subjects with values from an experiment in which a known amount of a substantially purified polynucleotide is used. Another method to identify a normal or standard profile for expression of any one of the angiogenic genes is through quantitative RT-PCR studies. RNA isolated from body cells of a normal individual, particularly RNA isolated from endothelial cells, is reverse transcribed and real-time PCR using oligonucleotides specific for the relevant gene is conducted to establish a normal level of expression of the gene. Standard values obtained in both these examples may be compared with values obtained from samples from patients who are symptomatic for a disorder. Deviation from standard values is used to establish the presence of a disorder.

Once the presence of a disorder is established and a treatment protocol is initiated, hybridization assays or quantitative RT-PCR studies may be repeated on a regular basis to determine if the level of expression in the patient begins to approximate that which is observed in the normal subject. The results obtained from successive assays may be used to show the efficacy of treatment over a period ranging from several days to months.

According to a further aspect of the invention there is provided the use of an angiogenic polypeptide as described above in the diagnosis or prognosis of an angiogenesis-related disorder associated with any one of angiogenic genes of the invention, or a predisposition to such disorders.

When a diagnostic or prognostic assay is to be based upon any relevant angiogenic polypeptide, a variety of approaches are possible. For example, diagnosis or prognosis can be achieved by monitoring differences in the electrophoretic mobility of normal and mutant proteins. Such an approach will be particularly useful in identifying mutants in which charge substitutions are present, or in which insertions, deletions or substitutions have resulted in a significant change in the electrophoretic migration of the resultant protein. Alternatively, diagnosis or prognosis may be based upon differences in the proteolytic cleavage patterns of normal and mutant proteins, differences in molar ratios of the various amino acid residues, or by functional assays demonstrating altered function of the gene products.

In another aspect, antibodies that specifically bind the relevant angiogenic gene product may be used for the diagnosis or prognosis of disorders characterized by abnormal expression of the gene, or in assays to monitor patients being treated with the relevant angiogenic gene or protein or agonists, antagonists, or inhibitors thereof. Antibodies useful for diagnostic or prognostic purposes may be prepared in the same manner as described above for therapeutics. Diagnostic or prognostic assays may include methods that utilize the antibody and a label to detect the relevant protein in human body fluids or in extracts of cells or tissues. The antibodies may be used with or without modification, and may be labelled by covalent or non-covalent attachment of a reporter molecule.

A variety of assays for measuring the relevant angiogenic polypeptide based on the use of antibodies specific for the polypeptide are known in the art and provide a basis for diagnosing altered or abnormal levels of expression. Normal or standard values for expression are established by combining body fluids or cell extracts taken from normal mammalian subjects, preferably human, with antibody to the relevant protein under conditions suitable for complex formation. The amount of standard complex formation may be quantitated by various methods which are known in the art. Examples include, but are not limited to, enzyme-linked immunosorbent assays (ELISAs), radioimmunoassays (RIAs), immunofluorescence, flow cytometry, histology, electron microscopy, in situ assays, immunoprecipitation, Western blot etc. For example, using the ELISA technique an enzyme which is bound to the antibody will react with an appropriate substrate, preferably a chromogenic substrate, in such a manner as to produce a chemical moiety that can be detected for example by spectrophotomeric, fluorimetric or by visual means. Detection may also be accomplished by using other assays such as RIAs where the antibodies or antibody fragments are radioactively labelled. It is also possible to label the antibody with a fluorescent compound. When the fluorescently labelled antibody is exposed to light of a certain wavelength, its presence can then be detected due to fluorescence. The antibody can also be detectably labelled by coupling it to a chemiluminescent compound. The presence of the chemiluminescent-tagged antibody is then determined by detecting the presence of luminescence that arises during the course of a chemical reaction.

Quantities of protein expressed in subject, control, and disease samples from biopsied tissues are compared with the standard values. Deviation between standard and subject values establishes the parameters for diagnosing or prognosing disease.

Once an individual has been diagnosed or prognosed with a disorder, effective treatments can be initiated, as described above. In the treatment of angiogenesis-related diseases which are characterised by uncontrolled or enhanced angiogenesis, the expanding vasculature needs to be inhibited. This would involve inhibiting the relevant angiogenic genes or proteins of the invention that promote angiogenesis. In addition, treatment may also need to stimulate expression or function of the relevant angiogenic genes or proteins of the invention whose normal role is to inhibit angiogenesis but whose activity is reduced or absent in the affected individual.

In the treatment of angiogenesis-related diseases which are characterised by inhibited or decreased angiogenesis, approaches which enhance or promote vascular expansion are desirable. This may be achieved using methods essentially as described above but will involve stimulating the expression or function of the relevant angiogenic gene or protein whose normal role is to promote angiogenesis but whose activity is reduced or absent in the affected individual. Alternatively, inhibiting genes or proteins that restrict angiogenesis may also be an approach to treatment.

Microarray

In further embodiments, complete cDNAs, oligonucleotides or longer fragments derived from any of the polynucleotide sequences described herein may be used as probes in a microarray. The microarray can be used to monitor the expression level of large numbers of genes simultaneously and to identify genetic variants, mutations, and polymorphisms. This information may be used to determine gene function, to understand the genetic basis of angiogenesis-related disorders, to diagnose or prognose angiogenesis-related disorders, and to develop and monitor the activities of therapeutic agents. Microarrays may be prepared, used, and analysed using methods known in the art. (For example, see Schena et al., 1996; Heller et al., 1997).

Transformed Hosts

The present invention also provides for the production of genetically modified (knock-out, knock-in and transgenic), non-human animal models comprising the nucleic acid molecules of the invention. These animals are useful for the study of the function of the relevant angiogenic gene, to study the process of angiogenesis, to study the mechanisms of angiogenic disease as related to these genes, for the screening of candidate pharmaceutical compounds for the treatment of angiogenesis-related disorders, for the creation of explanted mammalian cell cultures which express the protein or mutant protein, and for the evaluation of potential therapeutic interventions.

Animal species which are suitable for use in the animal models of the present invention include, but are not limited to, rats, mice, hamsters, guinea pigs, rabbits, dogs, cats, goats, sheep, pigs, and non-human primates such as monkeys and chimpanzees. For initial studies, genetically modified mice and rats are highly desirable due to the relative ease in generating knock-in, knock-out or transgenics of these animals, their ease of maintenance and their shorter life spans. For certain studies, transgenic yeast or invertebrates may be suitable and preferred because they allow for rapid screening and provide for much easier handling. For longer term studies, non-human primates may be desired due to their similarity with humans.

To create an animal model based on any one of the angiogenic genes of the invention, several methods can be employed. These include, but are not limited to, generation of a specific mutation in a homologous animal, gene, insertion of a wild type human gene and/or a humanized animal gene by homologous recombination, insertion of a mutant (single or multiple) human gene as genomic or minigene cDNA constructs using wild type, mutant or artificial promoter elements, or insertion of artificially modified fragments of the endogenous gene by homologous recombination. The modifications include insertion of mutant stop codons, the deletion of DNA sequences, or the inclusion of recombination elements (lox p sites) recognized by enzymes such as Cre recombinase.

To create transgenic mice in order to study gain of gene function in vivo, any relevant angiogenic gene can be inserted into a mouse germ line using standard techniques such as oocyte microinjection. Gain of gene function can mean the overexpression of a gene and its protein product, or the genetic complementation of a mutation of the gene under investigation. For oocyte injection, one or more copies of the wild type or mutant gene can be inserted into the pronucleus of a just-fertilized mouse oocyte. This oocyte is then reimplanted into a pseudo-pregnant foster mother. The liveborn mice can then be screened for integrants using analysis of tail DNA for the presence of the relevant human angiogenic gene sequence. The transgene can be either a complete genomic sequence injected as a YAC, BAC, PAC or other chromosome DNA fragment, a cDNA with either the natural promoter or a heterologous promoter, or a minigene containing all of the coding region and other elements found to be necessary. for optimum expression.

To generate knock-out mice or knock-in mice, gene targeting through homologous recombination in mouse embryonic stem (ES) cells may be applied. Knock-out mice are generated to study loss of gene function in vivo while knock-in mice allow the study of gain of function or to study the effect of specific gene mutations. Knock-in mice are similar to transgenic mice however the integration site and copy number are defined in the former.

For knock-out mouse generation, gene targeting vectors can be designed such that they disrupt (knock-out) the protein coding sequence of the relevant angiogenic gene in the mouse genome. Knock-out animals of the invention will comprise a functional disruption of a relevant angiogenesis gene of the invention such that the gene does not express a biologically active product. It can be substantially deficient in at least one functional activity coded for by the gene. Expression of the polypeptide encoded by the gene can be substantially absent (i.e. essentially undetectable amounts are made) or may be deficient in activity such as where only a portion of the gene product is produced. In contrast, knock-in mice can be produced whereby a gene targeting vector containing the relevant angiogenic gene can integrate into a defined genetic locus in the mouse genome. For both applications, homologous recombination is catalysed by specific DNA repair enzymes that recognise homologous DNA sequences and exchange them via double crossover.

Gene targeting vectors are usually introduced into ES cells using electroporation. ES cell integrants are then isolated via an antibiotic resistance gene present on the targeting vector and are subsequently genotyped to identify those ES cell clones in which the gene under investigation has integrated into the locus of interest. The appropriate ES cells are then transmitted through the germline to produce a novel mouse strain.

In instances where gene ablation results in early embryonic lethality, conditional gene targeting may be employed. This allows genes to be deleted in a temporally and spatially controlled fashion. As above, appropriate ES cells are transmitted through the germline to produce a novel mouse strain, however the actual deletion of the gene is performed in the adult mouse in a tissue specific or time controlled manner. Conditional gene targeting is most commonly achieved by use of the cre/lox system. The enzyme cre is able to recognise the 34 base pair loxP sequence such that loxP flanked (or floxed) DNA is recognised and excised by cre. Tissue specific crew expression in transgenic mice enables the generation of tissue specific knock-out mice by mating gene targeted floxed mice with cre transgenic mice. Knock-out can be conducted in every tissue (Schwenk et al., 1995) using the ‘deleter’ mouse or using transgenic mice with an inducible cre gene (such as those with tetracycline inducible cre genes), or knock-out can be tissue specific for example through the use of the CD19-cre mouse (Rickert et al., 1997).

According to still another aspect of the invention there is provided the use of genetically modified non-human animals for the screening of candidate pharmaceutical compounds.

It will be clearly understood that, although a number of prior art publications are referred to herein, this reference does not constitute an admission that any of these documents forms part of the common general knowledge in the art, in Australia or in any other country. Throughout this specification and the claims, the words “comprise”, “comprises” and “comprising” are used in a non-exclusive sense, except where the context requires otherwise.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Example of the expression profile of selected differentially expressed clones during defined time points in the in vitro model of angiogenesis. Time points at the defined stages of 0.5 hours, 3 hours, 6 hours and 24 hours of the in vitro tube formation assay were plotted against the log ratio of cy5 (red) and cy3 (green) dyes used for microarray hybridizations. A: example of a clone with peak expression at the 0.5 hour time point; B: example of a clone with peak expression at the 3 hour time point; C: example of a clone with peak expression at the 6 hour time point; and D: example of a clone with peak expression at the 24 hour time point.

FIG. 2. Expression profile of differentially expressed genes BNO782 and BNO481. Both genes show peak expression at the 6 hour time point of the in vitro tube formation assay. A: BNO782; B: BNO481.

FIG. 3. Analysis of the level of BNO782 expression knock-down mediated by BNO782 siRNA2 and BNO481 expression knock-down mediated by BNO481 siRNA1, as measured by real-time RT-PCR. The three siRNA oligonucleotides targeted to each gene were able to reduce -expression of the gene to varying degrees with BNO781 siRNA2 inhibiting BNO781 expression by 24% (A) and BNO481 siRNA1 inhibiting expression of BNO481 by 36% (B).

FIG. 4. Reducing BNO782 or BNO481 mRNA expression inhibits HUVEC tube formation. HUVECs infected with BNO782 siRNA2, BNO481 siRNA1, or a vector control were plated on Matrigel for 24hrs. Vector infected cells formed extensive networks of tube structures (A and C). In contrast, cells infected with BNO782 siRNA2 or BNO481 siRNA1 exhibited tube structure networks of significantly reduced complexity with a high number of incomplete tube extensions (B and D).

MODES FOR PERFORMING THE INVENTION Example 1 In Vitro Capillary Tube Formation

The in vitro model of angiogenesis is essentially as described in Gamble et al (1993). The assay was performed in collagen under the stimulation of phorbol myristate acetate (PMA) and the anti-integrin (α₂β₁) antibody, RMACII. Human umbilical vein endothelial cells (HUVECs) were used in all experiments between passages 2 to 4.

Cells were harvested from bulk cultures (t=0), replated onto the collagen gels with stimulation and then harvested from the collagen gels at 0.5, 3.0, 6.0 and 24 hours after commencement of the assay. These time points were chosen since major morphological changes occur at these stages. Briefly, by 0.5 hours, cells have attached to the collagen matrix and have commenced migration into the gel. By 3.0 hours, small intracellular vesicles are visible. By 6.0 hours, these vesicles are coalescing together to form membrane bound vacuoles and the cells in the form of short sprouts have invaded the gel. After this time, these vacuoles fuse with the plasma membrane, thus expanding the intercellular space to generate the lumen (Meyer et al., 1997). The formation of these larger vacuoles is an essential requirement of lumen formation (Gamble et al., 1999). By 24 hours, the overall anastomosing network of capillary tubes has formed and has commenced degeneration.

Example 2 RNA Isolation, cDNA Synthesis and Amplification

Cells harvested at the specified time points were used for the isolation of total RNA using the Trizol reagent (Gibco BRL) according to manufacturers conditions. SMART (Switching mechanism at 5′ end of RNA transcript) technology was used to convert small amounts of total RNA into enough cDNA to enable cDNA subtraction to be performed (see below). This was achieved using the SMART-PCR cDNA synthesis kit (Clontech-user manual PT3041-1) according to manufacturers recommendations. The SMART-PCR cDNA synthesis protocol generated a majority of full length cDNAs which were subsequently PCR amplified for cDNA subtraction.

Example 3 Suppression Subtractive Hybridization (SSH)

SSH was performed on SMART amplified cDNA in order to enrich for cDNAs that were either up-regulated or down-regulated between the cDNA populations defined by the selected time-points. This technique also allowed “normalisation” of the regulated cDNAs, thereby making low abundance cDNAs (i.e. poorly expressed, but important, genes) more easily detectable. To do this, the PCR-Select cDNA synthesis kit (Clontech-user manual PT3041-1) and PCR-Select cDNA subtraction kit (Clontech-user manual PT1117-1) were used based on manufacturers conditions.

These procedures relied on subtractive hybridization and suppression PCR amplification. SSH was performed between the following populations: 0-0.5 hours; 0.5-3.0 hours; 3.0-6.0 hours; 6.0-24 hours.

Example 4 Differential Screening of cDNA Clones

Following SSH, the cDNA fragments were digested with EagI and cloned into the compatible unique NotI site in pBluescript KS⁺ using standard techniques (Sambrook et al., 1989). This generated forward and reverse subtracted libraries for each time period. Initially, the forward subtracted libraries were used in subsequent studies to identify those clones representing genes that were up-regulated in their expression during the in vitro model of angiogenesis. To do this, a microarray analysis procedure was adopted.

Microarray Slide Preparation

A total of 10,000 clones from the 4 forward subtracted libraries (3,200 clones from 0-0.5 hr; 3,000 clones from 0.5-3 hr; 2,800 clones from 3-6 hr; 1,000 clones from 6-24 hr) were chosen to construct microarray slides. Inserts from these clones were amplified using standard PCR techniques with flanking T3 and T7 pBluescript KS+vector primers. DNA from each clone was spotted in duplicate onto a single microarray slide. Appropriate positive and negative controls were also incorporated onto the plate.

Probe Labelling

Human umbilical vein endothelial cells harvested at the specified time points (0, 0. 5, 3, 6, and 24 hr) were used for the isolation of total RNA using the Trizol reagent (Gibco BRL) according to manufacturers conditions. From each time point, 0.5 ug of total RNA was used as a template for the amplification of antisense RNA (aRNA) using the Ambion MessageAmp™ aRNA Kit. Briefly, total RNA was reversed transcribed with a T7 oligo(dT) primer in order to synthesize cDNA containing a T7 promoter sequence extending from the poly(A) tails of messages generated by reverse transcription. The cDNA was converted to a double-stranded DNA template and used for in vitro transcription of aRNA, incorporating 5-(3-aminoallyl)-UTP so as to allow coupling of fluorescent CyDyes. A typical amplification reaction would yield approximately 10 ug of mRNA (>400× amplification, assuming the initial total RNA contained <5% mRNA).

Microarray Hybridization

After coupling of CyDyes, the synthesized aRNA was used as a probe (3.0-3.5 ug) for hybridization to a microarray slide. The hybrizations performed were as follows:

1. 0 vs 0.5 h (6 slides, 3 Dye swaps)

2. 0 vs 3 h (4 slides, 2 Dye swaps)

3. 0 vs 6 h (4 slides, 2 Dye swaps)

4. 0 vs 24 h (4 slides, 2 Dye swaps)

Multiple slides were hybridized for each time point in order to verify the result from any one hybridization. Slides were hybridized in chambers for 16 hours, washed, and then scanned using the GenePix 2000 scanner. Those clones that were shown to be highly up-regulated were chosen for further analysis.

In summary, SSH was used in combination with microarray analyses to identify genes that are up-regulated and may be involved in biological processes underlying endothelial cell activation and blood vessel formation. This approach is novel in that it involves nucleotide hybridization steps that aim to reduce gene detection redundancy and enhance the chances of detecting; genes that are of low overall representation in the endothelial cell transcriptome. The nucleotide-based sequential time-points aims to detect the timepoint at which the up-regulation of a particular gene takes place in a way that reduces redundancy of detection. For example, a gene that is up-regulated at 3 hrs, and its expression remains up-regulated in subsequent time-points, will only be detected in the 0.5-3 hr subtraction step. In contrast, if subtractions were done with the 0 hr timepoint for all subsequent timepoints then this example gene would be detected at all subtraction steps following the 3 hrs timepoint subtraction. This would introduce redundancy that could result in masking the possible detection of other genes of lower representation in the endothelial cell mRNA expression pool. The subsequent use of microarray analysis is based on the comparison subtraction hybridization in the SSH step involving each timepoint with the 0 hrs timepoint. This enables the expression profiling of each gene across all timepoints in relation to 0 hrs, irrespective of the timepoint at which it is up-regulated.

Example 5 Clone Selection

From analysis of the microarray hybridizations, a total of 1,963 clones were identified to be up-regulated in their expression at specified time points during the in vitro model of angiogenesis. FIG. 1 provides an example of the expression profiles observed during defined time points in the in vitro model for a selection of clones. Each of the 1,963 clones were sequenced and subsequent in silico database analysis was used to remove clones containing vector sequences only and clones for which. poor sequence was obtained. Following this, redundancy screens were used to group clones according to individual genes that they represented. This left a total of 523 genes that were found to be up-regulated in their expression during the process of angiogenesis.

Tables 1, 2 and 3 provide information on the up-regulated clones that were sequenced. Table 1 includes those clones which represent previously uncharacterised or novel genes, while Table 2 includes clones that correspond to previously identified genes which have not before been associated with angiogenesis. Also identified were a number of genes that have previously been shown to be involved in the process of angiogenesis (Table 3). The identification of these clones provides a validation or proof of principle of the effectiveness of the angiogenic gene identification strategy employed and suggests that the clones listed in Tables 1 and 2 are additional angiogenic gene candidates.

Example 6 Analysis of the Angiogenic Genes

Further evidence for the involvement of the genes in Tables 1 and 2 in angiogenesis can be obtained through the functional analysis of each gene, for example by examining the effect that knock-down of their expression has on endothelial cell (EC) function and capillary tube formation.

A number of knock-down technologies and assays may be used. For example full-length coding sequences of the genes can be cloned into suitable expression vectors such as retroviruses or adenoviruses in both sense and anti-sense orientations and used for infection into ECs. Retrovirus infection gives long-term EC lines expressing the gene of interest whereas adenovirus infection gives transient gene expression. Infected cells can then be subjected to a number of EC assays including proliferation and capillary tube formation to confirm the role of each gene in angiogenesis.

In this study RNA interference (RNAi) gene knock-down technology was used for the analysis of gene function (see detailed description below). In this technique, short gene-specific RNA oligonucleotides are delivered to ECs in culture mediated by retroviral infection. These oligonucleotides bind to the gene transcript under study and induce its degradation resulting in silencing or reduction of gene expression. The consequences of this alteration to gene expression can be subsequently studied using assays that examine the ability of ECs to proliferate, migrate and form capillaries in vitro. The RNAi procedure adopted in this study is described below in detail and documents the analysis of two of the identified up-regulated angiogenesis genes. One of these genes is BNO782 shown in Table 1, a novel gene whose expression peaks at the 6 hour time point of the in vitro angiogenesis model (FIG. 2A), while the other gene is BNO481 (KPNA4) as shown in Table 2, which is a previously identified gene that has not before been shown to have a role in angiogenesis. The expression of BNO481 also peaks at the 6 hour time point of the in vitro angiogenesis model (FIG. 2B).

RNAi Oligonucleotide Design

Short interfering RNA (siRNA) oligonucleotides for RNAi-mediated knock-down of BNO782 and BNO481 were identified through application of in-house computer software. This software incorporates a series of parameters for selecting appropriate siRNA oligonucleotides. These parameters ensure that the siRNA sequence starts after an AA dinucleotide, the siRNA is in the open reading frame of the gene and 100 bp downstream the ATG start codon, the GC content of the siRNA is between 35% and 60%, and the siRNA does not have stretches of more than three T, A, C or G nucleotides. siRNA sequences that harbour low complexity regions were not used. In addition, BLAST analysis was used to select against probes that cross-hybridize with a number of genes (Blastn_refseq at “expect 500” and “word size 7” and alignment scores accepted at 19>score>15 where: alignment score=length_match−(gap+mismatch). siRNAs were synthesised in hair-pin format for cloning into retroviral vectors. For each gene, three siRNA oligonucleotides were selected with each one being examined individually for their effects on gene-knock-down and EC function.

Retroviral Infection of HUVE Cells

Each siRNA oligonucleotide was cloned into a retroviral vector for the delivery of the oligonucleotide to human umbilical vein endothelial cells (HUVECs). The siRNA vector was constructed through a modification of pMSCVpuro (BD Biosciences). Briefly, the 3′LTR of pMSCVpuro was inactivated by removal of the XbaI/NheI fragment. A H1-RNA Polymerase III promoter cassette was then inserted into the MCS of the vector. Annealed siRNA primers were ligated into the modified vector (pMSCVpuro(H1)) digested with BglII and HindIII restriction enzymes.

For virus production prior to infection of HUVECs, 293T cells were plated at a density of 1×10⁶ cells per well of a 6 well plate 18-24 hours before transfection in RPMI media (Invitrogen) supplemented with 10% FCS (Invitrogen) and 1.0 M Hepes (Invitrogen) without antibiotics. Cells were co-transfected with 2 μg retroviral DNA and 1.5 μg pVPack-VSV-G (Stratagene), 1.5 μg pVPack-GP (Stratagene) using Lipofectamine 2000 reagent (Invitrogen). Transfected cells were incubated overnight in 5% CO₂ at 37° C. The following day, media containing the DNA/LF2000 complexes was removed and replaced with RPMI supplemented with 10% FCS, 1.0 M Hepes and 1% PSG (Invitrogen). Virus containing supernatants were collected 48-72 hours post transfection and filtered using a 0.45 μM filter. Virus was aliquoted and stored at −80° C.

For the retroviral infection of HTJVECs (Clonetics), cells were plated 24 hours before infection in EGM-2 media (Clonetics) at a density of 1.3×10⁵ cells per well of a 6 well plate. The following day, 500 μl of virus supernatant was combined with 500 μl of EGM-2 complete media. Polybrene (Sigma) was added to a final concentration of 8.0 μg/ml. Media was aspirated from the cells and replaced with the viral mix. Cells were incubated with the viral mix in 5% CO₂ at 37° C. After 3 hours incubation, an additional 1.0 ml of EGM-2 media was added and cells were incubated for a further 24 hours. After this time HUVE cells were split 1:2 and replated into a 6 well plate. Cells were incubated for 24 hours following splitting to allow them to recover and adhere. To select for infected cells, medium was replaced with EGM-2 complete medium containing puromycin (Sigma) at a 0.4 μg/ml final concentration. Cells were incubated until uninfected cells treated with puromycin had died and infected resistant cells had grown to confluence. Media containing puromycin was replaced every 48 hours to replenish puromycin and remove cell debris. Once resistant cells were grown to confluence (approximately 4-5 days after starting selection), cells were washed in PBS, trypsinised and their properties analysed using the Matrigel capillary tube formation assay.

Capillary Tube Formation Assay

96 well tissue culture plates were coated with 50 μl of cold Matrigel (BD Biosciences) at 4° C. in a two layer process. Matrigel was allowed to polymerize at 37° C. for a minimum of 30 minutes before being used. Trypsinised cells were collected in 500 μl of EGM-2 media then centrifuged at 400 rcf for 3 minutes to pellet cells. This allows for the removal of trypsin that may interfere with the assay. Cell pellets were resuspended in 500 μl EGM-2 media then counted using a heamocytometer. Cells were diluted to 2.5×10⁵ cells/ml in EGM-2 media. 100 μl of the diluted cell suspension was added to duplicate Matrigel coated wells. The final cell density was 25,000 cells/well. Plates were incubated for 22 hours in a humidified incubator at 37° C. with 5% CO₂. Images were obtained using an Olympus BX-51 microscope with a 4× objective and Optronics MagnaFire software. Remaining cells were pelleted at 400 rcf for 3 minutes, then media was removed and pellets stored at −80° C. for extraction of RNA for real-time RT-PCR analysis (see below). For all assays performed, a vector control was included. This consisted of HUVECs undergoing the infection and selection process with virus made for the vector containing no siRNA insert. This allows for comparison of capillary tube formation ability between a control (vector) and the individual siRNA under analysis.

Real-Time RT-PCR Analysis

To determine the level of gene knock-down (mediated by the siRNAs) occurring in the HUVECs, real-time RT-PCR was employed. This involved isolation of RNA from infected cells using the RNeasy Mini or Midi kits (Qiagen) as per manufacturer's instructions (including the on-column DNase treatment). Total RNA was visualised on a 1.2% TBE agarose gel containing ethidium bromide to check for quality and purity. Total RNA concentration was determined by A₂₆₀ on a spectrophotometer.

For the synthesis of cDNA, total RNA (at least lug and preferably at a concentration >1.0 ug/ul) was reverse transcribed using M-MLV (Promega) as per manufacturer's directions. Briefly, the RNA sample to be analysed was made up to 13 ul with water and 1.0 ul of oligo-dT primer (500 ng/ul) was added. After incubating at 70° C. for 5 minutes, the tubes were placed on ice for 5 minutes and 11 ul of a pre-made master mix containing 5.0 ul M-MLV RT 5× Reaction Buffer, 1.25 ul 10 mM dNTP mix, 1.0 ul of M-MLV RT (H⁻ point mutant) enzyme, and 3.75 ul water was added. This mix was incubated at 40° C. for one hour, and the reaction terminated by incubating at 70° C. for 15 minutes.

Real-Time PCRs were run on the RotorGene™ 2000 system (Corbett Research). Reactions used AmpliTaq Gold enzyme (Applied Biosystems) and followed the manufacturers instructions. Real-Time PCR reactions were typically performed in a volume of 25 ul and consisted of 1× AmpliTaq Gold Buffer, 200 nM dNTP mix, 2.0 mM MgCl₂ (may vary for primer combination used), 0.3 uM of each primer, 1×SYBR Green mix (Cambrex BioScience Rockland Inc), 1.2 ul of AmpliTaq Gold Enzyme, and 10 ul of a 1 in 5 dilution of the cDNA template.

Cycling conditions were typically performed at 94° C. for 12 minutes, followed by 35 cycles of 94° C. for 15 seconds, 60° C. for 15 seconds, and 72° C. for 20 seconds. The annealing temperature of the primers may vary depending on the properties of the primers used.

The PCR cycling was followed by the generation of a melt curve using the RotorGene™ 2000 software where the amount of annealed product was determined by holding at each degree between 50° C. and 99° C. and measuring the absorbance. All products were run on a 1.2% agarose gel containing ethidium bromide to check specificity in addition to observing the melt curve.

The level of knock-down of a particular gene was then measured by a comparison of its expression level in HUVECs infected with the relevant siRNA under investigation as opposed to HUVECs infected with the retroviral vector alone.

In Vitro Regulation of HUVEC Function—BNO782 and BNO481

The siRNA oligonucleotides designed to knock-down BNO782 and BNO481 expression are represented by SEQ ID Numbers: 45-47 and SEQ ID Numbers: 48-50 respectively. Real-time RT-PCR analysis of HUVECs retrovirally infected with these siRNAs revealed that each siRNA was able to knock-down the expression of BNO782 or BNO481 to varying degrees. The level of BNO782 expression knock-down mediated by BNO782 siRNA2 (SEQ ID NO: 46) was 24% (FIG. 3A), while expression of BNO481 was reduced by 36% (FIG. 3B) using BNO481 siRNA1 (SEQ ID NO: 48). Both of these siRNAs were subsequently used separately in Matrigel assays to examine the effects that this level of knock-down for each gene had on the ability of HUVECs to participate in capillary tube formation. As can be seen in FIG. 4, reducing BNO782 or BNO481 mRNA levels inhibits HUVEC tube formation. Vector infected cells formed extensive networks of tube structures (FIGS. 4A and 4C) while cells infected with BNO782 siRNA2 or BNO481 siRNA1, exhibited tube structure networks of significantly reduced complexity with a high number of incomplete tube extensions (FIGS. 4B and 4D). This result confirms a role for both BNO782 and BNO481 in the process of angiogenesis.

Protein Interaction Studies

The ability of any one of the angiogenic proteins of the invention, including BNO782 and BNO481, to bind known and unknown proteins can be examined. Procedures such as the yeast two-hybrid system are used to discover and identify any functional partners. The principle behind the yeast two-hybrid procedure is that many eukaryotic transcriptional activators, including those in yeast, consist of two discrete modular domains. The first is a DNA-binding domain that binds to a specific promoter sequence and the second is an activation domain that directs the RNA polymerase II complex to transcribe the gene downstream of the DNA binding site. Both domains are required for transcriptional activation as neither domain can activate transcription on its own. In the yeast two-hybrid procedure, the gene of interest or parts thereof (BAIT), is cloned in such a way that it is expressed as a fusion to a peptide that has a DNA binding domain. A second gene, or number of genes, such as those from a cDNA library (TARGET), is cloned so that it is expressed as a fusion to an activation domain. Interaction of the protein of interest with its binding partner brings the DNA-binding peptide together with the activation domain and initiates transcription of the reporter genes. The first reporter gene will -select for yeast cells that contain interacting proteins (this reporter is usually a nutritional gene required for growth on selective media) The second reporter is used for confirmation and while being expressed in response to interacting proteins it is usually not required for growth.

The nature of the interacting genes and proteins can also be studied such that these partners can also be targets for drug discovery.

Structural Studies

Recombinant angiogenic proteins of the invention can be produced in bacterial, yeast, insect and/or mammalian cells and used in crystallographical and NMR studies. Together with molecular modeling of the protein, structure-driven drug design can be facilitated. TABLE 1 Novel Angiogenesis Genes BNO UniGene GenBank Peak Number Symbol Gene Description - Homology Number Number Expression (h) BNO605 BNO605 EST, UI-HF-BR0p-ajy-c-08-0-UI.s1 Homo sapiens cDNA None AW576601 BNO612 FLJ20445 hypothetical protein FLJ20445 Hs.343748 NM_017824 6 BNO616 MGC2747 hypothetical protein MGC2747 Hs.194017 NM_024104 0.5, 6   BNO617 FLJ20986 hypothetical protein FLJ20986 Hs.324507 NM_024524 6 BNO618 FLJ14834 hypothetical protein FLJ14834 Hs.62905 NM_032849 3 BNO620 FLJ22746 hypothetical protein FLJ22746 Hs.147585 NM_024785 0.5 BNO622 KIAA1376 KIAA1376 protein Hs.24684 BC015928 3, 24 BNO627 BNO627 EST, AV756199 BM Homo sapiens cDNA clone BMFAUH02 5′ None SEQ ID NO: 1 6 BNO628 BNO628 EST, QV1-BT0631-130300-111-e03 BT0631 Homo sapiens cDNA None SEQ ID NO: 2 6 BNO629 BNO629 EST, Homo sapiens cDNA clone IMAGE: 2664022 3′ None SEQ ID NO: 3 6 BNO630 BNO630 EST, Homo sapiens cDNA clone IMAGE: 2357465 3′ None SEQ ID NO: 4, 51 6 BNO632 BNO632 ESTs Hs.404198 SEQ ID NO: 5 6 BNO633 BNO633 ESTs, Weakly similar to hypothetical protein FLJ20378 Hs.310598 SEQ ID NO: 6 24 BNO634 BNO634 ESTs Hs.345443 SEQ ID NO: 7 6 BNO635 BNO635 Hypothetical protein Hs.54347 BC057847 6 BNO636 BNO636 ESTs Hs.105636 SEQ ID NO: 8 3 BNO637 BNO637 ESTs Hs.486928 SEQ ID NO: 9, 52 6 BNO638 BNO638 EST None SEQ ID NO: 10 6 BNO639 BNO639 None None SEQ ID NO: 11, 53 6 BNO640 BNO640 None None SEQ ID NO: 12 6 BNO645 FLJ10498 hypothetical protein FLJ10498 Hs.270107 NM_018115 24 BNO648 LOC57146 hypothetical protein from clone 24796 Hs.27191 NM_020422 0.5 BNO652 FLJ31051 hypothetical protein FLJ31051 Hs.406199 NM_153687 6 BNO655 LOC51122 HSPC042 protein Hs.432729 NM_016094 3 BNO659 FLJ32123 FLJ32123 Hs.349397 AK056685 6 BNO662 BNO662 ESTs Hs.444495 BX647355 6 BNO664 FLJ10312 FLJ10312 None NM_030672 3 BNO669 BNO669 ESTs Hs.172998 BC030094 3 BNO671 KIAA0882 KIAA0882 protein Hs.411317 AB020689 3 BNO673 BNO673 hypothetical protein DKFZp434L142 Hs.323583 NM_016613 6 BNO675 FLJ10700 hypothetical protein FLJ10700 Hs.295909 NM_018182 3 BNO677 FLJ30135 FLJ30135 Hs.34906 BC020494 3, 24 BNO685 FLJ10849 hypothetical protein FLJ10849 Hs.386784 NM_018243 BNO687 MGC45416 hypothetical protein MGC45416 Hs.95835 NM_152398 24 BNO690 C15orf15 chromosome 15 open reading frame 15 Hs.274772 NM_016304 3 BNO694 BNO694 cDNA DKFZp566E0124 None AL050030 6 BNO697 BNO697 Hypothetical protein MGC45871 Hs.345588 BC014203 24 BNO700 C7orf30 chromosome 7 open reading frame 30 Hs.87385 NM_138446 24 BNO704 KIAA1102 KIAA1102 protein Hs.156761 AB029025 BNO705 BNO705 ESTs Hs.30280 SEQ ID NO: 13 3 BNO706 LOC116441 hypothetical protein BC014339 Hs.22026 NM_138786 24 BNO708 BNO708 ESTs Hs.12876 SEQ ID NO: 14 6 BNO710 BNO710 FLJ23228 Hs.170623 AK026881 6 BNO712 BNO712 FLJ21592 Hs.5921 AK025245 3 BNO713 KIAA0970 KIAA0970 protein Hs.103329 NM_014923 6 BNO714 KIAA0121 KIAA0121 gene product Hs.155584 D50911 6 BNO723 C14orf123 chromosome 14 open reading frame 123 Hs.279761 NM_014169 6 BNO725 KIAA0582 KIAA0582 protein Hs.146007 NM_015147 24 BNO730 BNO730 ESTs Hs.158753 SEQ ID NO: 15 6 BNO731 C6orf166 chromosome 6 open reading frame 166 Hs.201864 NM_018064 3 BNO735 FLJ32029 Unnamed protein product Hs.26612 NM_173582 6 BNO737 BNO737 hypothetical protein DKFZp434F0318 Hs.23388 NM_030817 BNO740 KIAA1728 KIAA1728 protein Hs.437362 AB051515 24 BNO742 BNO742 hypothetical protein FLJ11795 Hs.84560 NM_024669 24 BNO745 BNO745 hypothetical protein DKFZp547A023 Hs.374649 NM_018704 6 BNO747 MGC23937 hypothetical protein MGC23937 similar to CG4798 Hs.91612 NM_145052 6 BNO753 BNO753 cDNA DKFZp667P1024 Hs.127811 AL832835 3 BNO754 KIAA0303 KIAA0303 protein Hs.212787 AB002301 3 BNO756 BNO756 ESTs Hs.443155 SEQ ID NO: 16, 54 BNO759 KIAA1416 KIAA1416 protein Hs.397426 AB037837 6 BNO761 C7orf24 chromosome 7 open reading frame 24 Hs.444840 NM_024051 6 BNO762 FLJ11223 cDNA FLJ11223 Hs.92308 AL832083 3 BNO768 FLJ30478 cDNA FLJ30478 Hs.298258 AK092048 6 BNO772 FLJ10525 Hypothetical protein FLJ10525 Hs.31082 NM_018126 6 BNO780 LOC58489 hypothetical protein from EUROIMAGE 588495 Hs.26765 AL390079 3 BNO782 MGC26717 Hypothetical protein Hs.406060 BC024188 6 BNO791 KIAA1053 KIAA1053 protein Hs.98259 NM_015589 6 BNO793 KIAA0766 KIAA0766 gene product Hs.28020 NM_014805 24 BNO795 BNO795 ESTs moderately similar to MDC-3.13 isoform 2 mRNA Hs.306343 AK123281 6 BNO800 KIAA1577 KIAA1577 protein Hs.449290 AB046797 6 BNO802 KIAA0877 KIAA0877 protein Hs.408623 AB020684 24 BNO812 KIAA0372 KIAA0372 gene product Hs.435330 NM_014639 6 BNO816 BNO816 cDNA clone 4052238 Hs.348514 BC014384 6 BNO818 MGC10067 hypothetical protein MGC10067 Hs.42251 NM_145049 3 BNO819 KIAA1191 KIAA1191 protein Hs.8594 NM_020444 24 BNO821 BNO821 ESTs Hs.87606 SEQ ID NO: 17 24 BNO825 FBXO30 F-box protein 30 Hs.421095 NM_032145 3 BNO831 C8orf1 chromosome 8 open reading frame 1 Hs.436445 NM_004337 24 BNO833 C6orf115 Chromosome 6 open reading frame 115 Hs.238205 BC014953 24 BNO838 BNO838 ESTs Hs.319095 SEQ ID NO: 18 3 BNO845 FLJ23728 cDNA FLJ23728 Hs.191094 AK074308 6 BNO848 C10orf45 Chromosome 10 open reading frame 45 Hs.103378 NM_031453 24 BNO849 BNO849 cDNA DKFZp434G0972 Hs.106148 AL133577 24 BNO852 CGI-111 CGI-111 protein Hs.11085 NM_016048 6 BNO856 LOC116068 hypothetical protein LOC116068 Hs.136235 AL832721 24 BNO857 C12orf2 chromosome 12 open reading frame 2 Hs.140821 NM_007211 6 BNO862 BNO862 DKFZP434C212 protein Hs.287266 AK023841 BNO868 BNO868 DKFZP566C134 protein Hs.20237 AB040922 3 BNO870 LOC57228 hypothetical protein from clone 643 Hs.206501 NM_020467 24 BNO871 KIAA1463 KIAA1463 protein Hs.21104 AB040896 6 BNO873 KIAA1376 KIAA1376 protein Hs.24684 NM_020801 0.5, 24   BNO876 FLJ10326 hypothetical protein FLJ10326 Hs.262823 NM_018060 24 BNO878 BNO878 hypothetical protein DKFZp761L1417 Hs.270753 NM_152913 6 BNO881 MGC11349 hypothetical protein MGC11349 Hs.288697 NM_025112 6 BNO883 FLJ39541 similar to RIKEN cDNA 9130404H11 gene Hs.21388 NM_178566 6 BNO886 BNO886 cDNA DKFZp686D04119 Hs.30258 BX537597 6 BNO887 KIAA0648 KIAA0648 protein Hs.31921 NM_015200 24 BNO890 KIAA1160 KIAA1160 protein Hs.512661 NM_020701 3 BNO892 C20orf108 chromosome 20 open reading frame 108 Hs.143736 NM_080821 3 BNO894 KIAA0205 KIAA0205 gene product Hs.528724 NM_014873 6 BNO895 C20orf112 chromosome 20 open reading frame 112 Hs.335142 NM_080616 0.5 BNO898 BNO898 clone IMAGE: 5243590 Hs.454832 BC036880 6 BNO905 KIAA1462 KIAA1462 protein Hs.192726 AB040895 3 BNO906 KIAA1199 KIAA1199 protein Hs.212584 AB033025 6 BNO908 C15orf12 chromosome 15 open reading frame 12 Hs.513041 NM_018285 BNO910 BNO910 cDNA DKFZp564F053 Hs.529772 AL049265 6 BNO917 BNO917 hypothetical protein dJ465N24.2.1 Hs.259412 NM_020317 24 BNO926 KIAA1238 KIAA1238 protein Hs.372288 AB033064 BNO928 BNO928 EST None SEQ ID NO: 19 3 BNO929 BNO929 EST None SEQ ID NO: 20 6 BNO930 BNO930 EST Hs.478376 SEQ ID NO: 21 6 BNO932 BNO932 EST Hs.492501 SEQ ID NO: 22, 55 3 BNO933 BNO933 EST None SEQ ID NO: 23 6 BNO934 BNO934 EST None SEQ ID NO: 24 6 BNO935 BNO935 EST None SEQ ID NO: 25 6 BNO936 BNO936 EST None SEQ ID NO: 26, 56 6 BNO937 BNO937 alpha gene sequence None AF203815 6 BNO938 BNO938 EST None SEQ ID NO: 27 0.5 BNO939 BNO939 EST None SEQ ID NO: 28 6 BNO940 BNO940 EST None SEQ ID NO: 29 6 BNO941 BNO941 EST None SEQ ID NO: 30 3 BNO942 BNO942 EST None SEQ ID NO: 31 6 BNO943 BNO943 EST None SEQ ID NO: 32 6 BNO944 BNO944 EST None SEQ ID NO: 33 6 BNO945 BNO945 EST None SEQ ID NO: 34 6 BNO946 BNO946 EST None SEQ ID NO: 35, 57 6 BNO948 BNO948 EST None SEQ ID NO: 36 6 BNO949 BNO949 EST None SEQ ID NO: 37, 58 3 BNO950 BNO950 EST None SEQ ID NO: 38 24 BNO951 BNO951 EST None SEQ ID NO: 39 24 BNO953 BNO953 EST None SEQ ID NO: 40 24 BNO961 BNO961 FLJ00138 protein Hs.199749 AK074067 3, 24 BNO1018 BNO1018 EST Hs.485935 SEQ ID NO: 41 3 BNO1019 BNO1019 EST None SEQ ID NO: 42 24 BNO1020 BNO1020 EST None SEQ ID NO: 43 3 BNO1021 BNO1021 EST None SEQ ID NO: 44 3

TABLE 2 Genes with a Previously Unknown Role in Angiogenesis BNO UniGene GenBank Peak Number Symbol Gene Description - Homology Number Number Expression (h) BNO436 NP nucleoside phosphorylase Hs.75514 NM_000270 6 BNO438 CD59 CD59 antigen p18-20 Hs.278573 NM_000611 24  BNO441 BIRC3 baculoviral IAP repeat-containing 3 Hs.127799 NM_001165 3 BNO442 FABP5 fatty acid binding protein 5 (psoriasis-associated) Hs.408061 NM_001444 24  BNO443 CBFB core-binding factor, beta subunit Hs.179881 NM_001755 6 BNO446 INHBA inhibin, beta A (activin A, activin AB alpha polypeptide) Hs.727 NM_002192 6 BNO447 MGST2 microsomal glutathione S-transferase 2 Hs.81874 NM_002413 24  BNO448 RAB6A RAB6A, member RAS oncogene family Hs.5636 NM_002869 6 BNO449 SAT spermidine/spermine N1-acetyltransferase Hs.28491 NM_002970 6 BNO451 TXNRD1 thioredoxin reductase 1 Hs.13046 NM_003330 6 BNO452 SLC4A7 solute carrier family 4, sodium bicarbonate cotransporter, member 7 Hs.132904 NM_003615 6 BNO453 PPAP2B phosphatidic acid phosphatase type 2B Hs.432840 NM_003713 3 BNO454 BCL10 B-cell CLL/lymphoma 10 Hs.193516 NM_003921 3 BNO455 DUSP1 dual specificity phosphatase 1 Hs.171695 NM_004417   0.5 BNO456 KIF5B kinesin family member 5B Hs.149436 NM_004521 6 BNO457 WTAP Wilms' tumour 1-associating protein Hs.119 NM_004906   0.5 BNO459 FOS v-fos FBJ murine osteosarcoma viral oncogene homolog Hs.25647 NM_005252   0.5 BNO460 GATA6 GATA binding protein 6 Hs.50924 NM_005257 3 BNO461 HRY hairy and enhancer of split 1, (Drosophila) Hs.250666 NM_005524   0.5 BNO462 SGK serum/glucocorticoid regulated kinase Hs.296323 NM_005627 3 BNO463 TIEG TGFB inducible early growth response Hs.82173 NM_005655   0.5 BNO464 BCAP31 B-cell receptor-associated protein 31 Hs.381232 NM_005745 BNO465 CALCRL calcitonin receptor-like Hs.152175 NM_005795 24  BNO466 SUI1 putative translation initiation factor Hs.150580 NM_005801 3 BNO467 TSC22 transforming growth factor beta-stimulated protein TSC-22 Hs.114360 NM_006022 6 BNO468 RAN RAN, member RAS oncogene family Hs.426035 NM_006325 BNO469 LYPLA1 lysophospholipase I Hs.12540 NM_006330 6 BNO470 SSFA2 sperm specific antigen 2 Hs.351355 NM_006751 6 BNO472 CLIC4 chloride intracellular channel 4 Hs.25035 NM_013943 24  BNO473 SLC7A11 solute carrier family 7, member 11 Hs.6682 NM_014331 3 BNO474 RAI14 retinoic acid induced 14 Hs.15165 NM_015577 6 BNO475 HSPC014 chromosome 13 open reading frame 12 Hs.279813 NM_015932 24  BNO476 UMP-CMPK UMP-CMP kinase Hs.11463 NM_016308 3 BNO477 SLC38A2 solute carrier family 38, member 2 Hs.298275 NM_018976 3 BNO478 ZNF317 zinc finger protein 317 Hs.18587 NM_020933 24  BNO479 RAB6C RAB6C, member RAS oncogene family Hs.333139 NM_032144 24  BNO480 MKI67IP MKI67 (FHA domain) interacting nucleolar phosphoprotein Hs.142838 NM_032390 3 BNO481 KPNA4 karyopherin alpha 4 (importin alpha 3) Hs.288193 NM_002268 3 BNO483 C14orf32 chromosome 14 open reading frame 32 Hs.406401 NM_144578 3 BNO484 SMARCA2 SWI/SNF related, matrix associated, regulator of chromatin, A2 Hs.198296 NM_003070   0.5 BNO485 SOX4 Homo sapiens SRY (sex determining region Y)-box 4 (SOX4), mRNA Hs.83484 NM_003107 3 BNO487 NR4A3 nuclear receptor subfamily 4, group A, member 3 Hs.80561 NM_006981   0.5 BNO488 NTN4 netrin 4 Hs.102541 NM_021229 BNO489 DNCI2 dynein, cytoplasmic, intermediate polypeptide 2 (DNCI2), mRNA Hs.66881 XM_027780   0.5 BNO490 UGCG UDP-glucose ceramide glucosyltransferase Hs.432605 NM_003358 0.5, 24   BNO491 P125 Sec23-interacting protein p125 Hs.300208 NM_007190 3 BNO492 NUDT4 nudix (nucleoside diphosphate linked moiety X)-type motif 4 Hs.355399 NM_019094 6 BNO495 SATB1 special AT-rich sequence binding protein 1 Hs.74592 NM_002971 6 BNO496 BZW1 basic leucine zipper and W2 domains 1 Hs.155291 NM_014670 3 BNO497 TDG thymine-DNA glycosylase Hs.173824 NM_003211 6 BNO498 ACTR3 ARP3 actin-related protein 3 homolog (yeast) Hs.380096 NM_005721 24  BNO499 LAMP2 lysosomal-associated membrane protein 2 Hs.8262 NM_013995 6 BNO500 ERBB2IP erbb2 interacting protein Hs.8117 NM_018695 6 BNO501 DNAJB6 DnaJ (Hsp40) homolog, subfamily B, member 6 Hs.181195 NM_005494 3 BNO502 EMP1 epithelial membrane protein 1 Hs.79368 NM_001423 6 BNO503 MAPK1 mitogen-activated protein kinase 1 Hs.324473 NM_002745 24  BNO504 CYP1A1 cytochrome P450, subfamily 1, polypeptide 1 Hs.72912 NM_000499 6 BNO505 ACVR1 activin A receptor, type I Hs.150402 NM_001105 3 BNO506 TPT1 tumor protein, translationally-controlled 1 Hs.401448 NM_003295 0.5, 24   BNO507 VAV3 vav 3 oncogene Hs.267659 NM_006113 3 BNO508 CAP adenylyl cyclase-associated protein Hs.104125 NM_006367 24  BNO509 HSPA5 Heat shock 70 kDa protein 5 (glucose-regulated protein, 78 kDa) Hs.75410 NM_005347 6 BNO510 TIA1 TIA1 cytotoxic granule-associated RNA binding protein Hs.239489 NM_022173 6 BNO511 CCNT2 cyclin T2 Hs.155478 NM_001241 6 BNO512 CHC1L chromosome condensation 1-like Hs.27007 NM_001268   0.5 BNO513 SFPQ splicing factor proline/glutamine rich Hs.180610 NM_005066 3 BNO514 PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha Hs.183037 NM_002734 24  BNO515 RALA v-ral simian leukemia viral oncogene homolog A (ras related) Hs.6906 NM_005402 6 BNO516 ANXA2 annexin A2 Hs.217493 NM_004039   0.5 BNO517 NUP153 nucleoporin 153 kDa Hs.211608 NM_005124 3 BNO518 RANBP9 RAN binding protein 9 Hs.279886 NM_005493 24  BNO519 PRPF4B PRP4 pre-mRNA processing factor 4 homolog B (yeast) Hs.198891 NM_003913 6 BNO520 TSN translin Hs.75066 NM_004622 6 BNO521 H3F3A H3 histone, family 3A Hs.181307 NM_002107 24  BNO523 PROS1 protein S (alpha) Hs.64016 NM_000313 6 BNO524 DDX3 DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 3 Hs.380774 NM_001356 3 BNO525 TCF4 transcription factor 4 Hs.359289 NM_003199 6 BNO526 PTP4A1 Protein tyrosine phosphatase type IVA, member 1 Hs.227777 NM_003463 6 BNO527 BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase) Hs.53250 NM_001204 3 BNO528 NFE2L2 nuclear factor (erythroid-derived 2)-like 2 Hs.155396 NM_006164 3 BNO531 AHR aryl hydrocarbon receptor Hs.170087 NM_001621 3 BNO532 RANBP7 RAN binding protein 7 Hs.5151 NM_006391 3 BNO533 ARF6 ADP-ribosylation factor 6 Hs.89474 NM_001663 3 BNO534 SCARF1 SCARF1 Scavenger receptor class F, member 1 Hs.57735 NM_003693E 24  BNO535 PLU-1 putative DNA/chromatin binding motif Hs.143323 NM_006618 24  BNO536 TOMM20 translocase of outer mitochondrial membrane 20 (yeast) homolog Hs.75187 NM_014765 6 BNO537 B2M beta-2-microglobulin Hs.48516 NM_004048 24  BNO538 zizimin1 zizimin1 Hs.8021 NM_015296 6 BNO539 ARPP-19 cyclic AMP phosphoprotein, 19 kD Hs.7351 NM_006628 3 BNO540 RAP1B RAP1B, member of RAS oncogene family Hs.156764 NM_015646 3 BNO541 MCP membrane cofactor protein Hs.83532 NM_153826 6 BNO542 IFI16 interferon, gamma-inducible protein 16 Hs.155530 NM_005531   0.5 BNO543 PRG1 proteoglycan 1, secretory granule Hs.1908 NM_002727 BNO544 KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog Hs.81665 NM_000222 0.5, 24   BNO545 SYBL1 synaptobrevin-like 1 Hs.24167 NM_005638 6 BNO546 TCF8 transcription factor 8 (represses interleukin 2 expression) Hs.232068 NM_030751E 6 BNO548 NXF1 nuclear RNA export factor 1 Hs.323502 NM_006362 3, 24 BNO549 RAP2B RAP2B, member of RAS oncogene family Hs.239527 NM_002886 3 BNO551 IL6ST interleukin 6 signal transducer (gp130, oncostatin M receptor) Hs.82065 NM_002184 6 BNO552 REST RE1-silencing transcription factor Hs.401145 NM_005612 6 BNO553 SLC19A2 solute carrier family 19 (thiamine transporter), member 2 Hs.30246 NM_006996 3 BNO554 EIF4G2 eukaryotic translation initiation factor 4 gamma, 2 Hs.183684 NM_001418 3 BNO555 PTPRE protein tyrosine phosphatase, receptor type, E Hs.31137 NM_006504 3 BNO556 PDE3A phosphodiesterase 3A, cGMP-inhibited Hs.777 NM_000921 3 BNO557 C1QR1 complement component 1, q subcomponent, receptor 1 Hs.97199 NM_012072 24  BNO558 RANBP2 RAN binding protein 2 Hs.199179 NM_006267 BNO559 KIS kinase interacting with leukemia-associated gene (stathmin) Hs.127310 NM_144624 24  BNO560 HMGCR 3-hydroxy-3-methylglutaryl-Coenzyme A reductase Hs.11899 NM_000859 6 BNO561 PDCD4 programmed cell death 4 (neoplastic transformation inhibitor) Hs.326248 NM_145341 3 BNO562 TACC1 transforming, acidic coiled-coil containing protein 1 Hs.173159 NM_006283   0.5 BNO564 DIS3 mitotic control protein dis3 homolog Hs.323346 NM_014953 6 BNO565 TOP2A topoisomerase (DNA) II alpha 170 kDa Hs.156346 NM_001067 6 BNO566 SLC7A2 solute carrier family 7, member 2 Hs.153985 NM_003046 6 BNO567 FH fumarate hydratase Hs.75653 NM_000143 6 BNO568 IL1RL1 interleukin 1 receptor-like 1 Hs.66 NM_003856 6 BNO569 HPRP3P U4/U6-associated RNA splicing factor Hs.11776 NM_004698 6 BNO570 DDX5 DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 5 Hs.76053 NM_004396 BNO571 MAD2L1 MAD2 mitotic arrest deficient-like 1 (yeast) Hs.79078 NM_002358 0.5, 24   BNO572 MADH7 MAD, mothers against decapentaplegic homolog 7 (Drosophila) Hs.100602 NM_005904 3 BNO573 E2F3 E2F transcription factor 3 Hs.1189 NM_001949 3 BNO574 CSNK2A2 CSNK2A2 Casein kinase 2, alpha prime polypeptide Hs.82201 NM_001896 6 BNO575 MAX MAX protein Hs.42712 NM_002382 6 BNO576 ERAP140 140 kDa estrogen receptor associated protein Hs.339283 AF493978 3 BNO577 CD9 CD9 antigen (p24) Hs.1244 NM_001769 24  BNO578 ATRX alpha thalassemia/mental retardation syndrome X-linked Hs.96264 NM_000489 6 BNO579 YWHAZ tyrosine/tryptophan activation protein, zeta polypeptide Hs.75103 NM_003406 3 BNO580 IDS iduronate 2-sulfatase (Hunter syndrome) Hs.172458 NM_000202 24  BNO581 SERPINE2 serine (or cysteine) proteinase inhibitor, clade E, member 2 Hs.21858 NM_006216 6 BNO582 DDEF1 development and differentiation enhancing factor 1 Hs.10669 NM_018482 6 BNO583 GLRX glutaredoxin (thioltransferase) Hs.28988 NM_002064 24  BNO584 MAP3K1 MAP3K1 Mitogen-activated protein kinase kinase kinase 1 Hs.170610 XM_042066 3 BNO585 ANKH ankylosis, progressive homolog (mouse) Hs.168640 NM_054027 3 BNO586 RBX1 ring-box 1 Hs.279919 NM_014248 24  BNO587 NAB1 NGFI-A binding protein 1 (EGR1 binding protein 1) Hs.107474 NM_005966 3 BNO588 TNFSF10 tumor necrosis factor (ligand) superfamily, member 10 Hs.83429 NM_003810 3 BNO589 PRDX3 peroxiredoxin 3 Hs.75454 NM_006793 6 BNO590 MAP2K1 mitogen-activated protein kinase kinase 1 Hs.3446 NM_002755 3 BNO591 NFATC1 nuclear factor of activated T-cells, calcineurin-dependent 1 Hs.96149 NM_006162 24  BNO594 USP7 ubiquitin specific protease 7 (herpes virus-associated) Hs.78683 NM_003470 BNO595 ARHB ras homolog gene family, member B Hs.406064 NM_004040 3 BNO596 PTEN phosphatase and tensin homolog Hs.10712 NM_000314 BNO597 UBL1 ubiquitin-like 1 (sentrin) Hs.81424 NM_003352 24  BNO598 RAB5A RAB5A, member RAS oncogene family Hs.73957 NM_004162 3 BNO599 ITGB1 integrin, beta 1 Hs.287797 NM_002211 24  BNO600 PRDM2 PR domain containing 2, with ZNF domain Hs.26719 NM_012231 6 BNO602 ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) Hs.271986 NM_002203 6 BNO603 ETV5 ets variant gene 5 (ets-related molecule) Hs.43697 NM_004454 3 BNO604 ZFHX1B zinc finger homeobox 1b Hs.34871 NM_014795 3 BNO606 LOC157713 lysophospholipase I-like pseudogene on chromosome 6 None NG_001063 BNO607 RBM3 RNA binding motif protein 3 Hs.301404 NM_006743   0.5 BNO609 NET-6 transmembrane 4 superfamily member tetraspan NET-6 Hs.364544 NM_014399 6 BNO610 EHD3 EH-domain containing 3 Hs.87125 NM_014600 24  BNO611 KIAA0992 palladin Hs.194431 NM_016081 6 BNO613 METL methyltransferase like 2 Hs.433213 NM_018396 3 BNO614 HT010 uncharacterized hypothalamus protein HT010 Hs.6375 NM_018471   0.5 BNO615 C3orf4 chromosome 3 open reading frame 4 Hs.107393 NM_019895 6 BNO619 RPL27A ribosomal protein L27a Hs.76064 NM_000990 6 BNO621 MIB Ubiquitin ligase mind bomb Hs.34892 AY149908   0.5 BNO623 KIAA0261 KIAA0261 protein Hs.154978 XM_042946 24  BNO624 KIAA1199 KIAA1199 protein Hs.50081 XM_051860 6 BNO625 HIF1 huntingtin interacting protein B Hs.6947 NM_014159 BNO642 ETL EGF-TM7-latrophilin-related protein Hs.57958 NM_022159 24  BNO643 VMP1 likely ortholog of rat vacuole membrane protein 1 Hs.166254 NM_030938 3 BNO644 TAF9 TATA box binding protein (TBP)-associated factor, 32 kDa Hs.60679 NM_016283 24  BNO646 MAN1A1 mannosidase, alpha, class 1A, member 1 Hs.432931 NM_005907 6 BNO647 DOCK4 Dedicator of cytokinesis 4 Hs.118140 NM_014705 24  BNO649 ADAMTS9 a disintegrin-like and metalloprotease (thrombospondin type 1 motif, 9) Hs.126855 NM_020249 24  BNO650 CSNK2A2 Casein kinase 2, alpha prime polypeptide Hs.82201 NM_001896 6 BNO651 RPLP0 ribosomal protein, large, P0 Hs.406511 NM_001002 6 BNO653 GALNT4 N-acetylgalactosaminyltransferase 4 Hs.271923 NM_003774 3 BNO654 GNG2 guanine nucleotide binding protein (G protein), gamma 2 Hs.289026 BC020774 6 BNO656 MBNL muscleblind-like (Drosophila) Hs.28578 NM_021038 BNO657 ARL8 ADP-ribosylation factor-like 8 Hs.25362 BC024163 3 BNO658 ASB3 ankyrin repeat and SOCS box-containing 3 Hs.9893 NM_016115 6 BNO660 GG2-1 TNF-induced protein Hs.17839 NM_014350 3 BNO661 ELL2 ELL-related RNA polymerase II, elongation factor Hs.98124 NM_012081 3 BNO663 ATP5J2 ATP synthase, H+ transporting, mitochondrial F0 complex, subunit f 2 Hs.235557 NM_004889 24  BNO665 SDCBP syndecan binding protein (syntenin) Hs.8180 NM_005625 3 BNO666 KIAA1959 Nm23-phosphorylated unknown substrate Hs.55067 NM_032873 3 BNO667 GNPNAT1 glucosamine-phosphate N-acetyltransferase 1 Hs.478025 NM_198066 6 BNO668 SPRED1 Sprouty-related, EVH1 domain containing 1 Hs.132804 NM_152594 3, 24 BNO670 Nbak2 homeodomain interacting protein kinase 1-like protein Hs.12259 NM_152696 6 BNO672 GABPA GA binding protein transcription factor, alpha subunit 60 kDa Hs.78 NM_002040 3 BNO674 V-1 likely ortholog of rat V-1 protein Hs.21321 NM_145808 24  BNO676 C8FW phosphoprotein regulated by mitogenic pathways Hs.7837 NM_025195 3 BNO678 TBC1D4 TBC1 domain family, member 4 Hs.173802 NM_014832 6 BNO679 ACATE2 likely ortholog of mouse acyl-Coenzyme A thioesterase 2 Hs.18625 NM_012332 24  BNO680 CRYZ crystallin, zeta (quinone reductase) Hs.83114 NM_001889 6 BNO681 KPNB1 karyopherin (importin) beta 1 Hs.180446 NM_002265 24  BNO682 RPL23A ribosomal protein L23a Hs.350046 NM_000984   0.5 BNO683 LIMS1 LIM and senescent cell antigen-like domains 1 Hs.112378 NM_004987 6 BNO684 WW45 WW45 protein Hs.288906 NM_021818 3 BNO686 ST3GALVI alpha2,3-sialyltransferase Hs.34578 NM_006100 6 BNO688 CPR8 cell cycle progression 8 protein Hs.283753 NM_004748 24  BNO689 HDCL hHDC for homolog of Drosophila headcase Hs.6679 NM_016217 3 BNO691 UBC ubiquitin C Hs.183704 NM_021009 3 BNO692 RDX radixin Hs.263671 NM_002906 24  BNO693 PELI1 pellino homolog 1 (Drosophila) Hs.7886 NM_020651 3 BNO695 MCC mutated in colorectal cancers Hs.1345 NM_002387 6 BNO696 RetSDR2 RetSDR2 Retinal short-chain dehydrogenase/reductase 2 Hs.282984 NM_016245 3 BNO698 CSS3 Chondroitin sulfate synthase 3 Hs.165050 AB086062 3 BNO699 BRE brain and reproductive organ-expressed (TNFRSF1A modulator) Hs.80426 NM_004899 6 BNO701 BAZ1A bromodomain adjacent to zinc finger domain, 1A Hs.8858 NM_013448 3 BNO702 HNRPDL heterogeneous nuclear ribonucleoprotein D-like Hs.372673 NM_005463 3 BNO703 PREI3 preimplantation protein 3 Hs.107942 NM_015387 6 BNO707 BNO707 Human XIST, coding sequence “a” Hs.83623 X56199 3 BNO709 ROD1 ROD1 regulator of differentiation 1 (S. pombe) Hs.374634 NM_005156 6 BNO711 SMAP-5 golgi membrane protein SB140 Hs.5672 NM_030799 6 BNO715 M-RIP Myosin phosphatase-Rho interacting protein Hs.430725 AB020671 0.5, 24   BNO716 HIVEP2 human immunodeficiency virus type I enhancer binding protein 2 Hs.75063 NM_006734 3 BNO717 DC42 hypothetical protein DC42 None NM_030921 3 BNO718 GRPEL2 GrpE-like 2, mitochondrial Hs.17121 NM_152407 6 BNO719 PCMF potassium channel modulatory factor Hs.5392 NM_020122 3 BNO720 UBE2E1 ubiquitin-conjugating enzyme E2E 1 (UBC4/5 homolog, yeast) Hs.163546 NM_003341 24  BNO721 KLHL4 kelch-like 4 (Drosophila) Hs.49075 NM_019117 BNO722 MANEA Mannosidase, endo-alpha Hs.46903 NM_024641 3 BNO724 TCF12 transcription factor 12 (HTF4, helix-loop-helix transcription factors 4) Hs.21704 NM_003205 6 BNO726 STAF42 SPT3-associated factor 42 Hs.435967 NM_053053 6 BNO727 CYFIP1 cytoplasmic FMR1 interacting protein 1 Hs.77257 NM_014608 6 BNO728 NOL5A nucleolar protein 5A (56 kDa with KKE/D repeat) Hs.376064 NM_006392 6 BNO729 GSA7 ubiquitin activating enzyme E1-like protein Hs.278607 NM_006395 6 BNO732 P66 Alpha P66 Alpha Hs.118964 NM_017660 BNO733 STAG1 stromal antigen 1 Hs.286148 NM_005862 BNO734 MYCT1 Myc target 1 Hs.18160 NM_025107 6 BNO736 SCAMP1 secretory carrier membrane protein 1 Hs.31218 NM_004866 3 BNO738 ACTG1 actin, gamma 1 Hs.14376 NM_001614   0.5 BNO739 HRB2 HIV-1 rev binding protein 2 Hs.154762 NM_007043 6 BNO741 VMP1 Likely orthologue of rat vacuole membrane protein 1 Hs.166254 NM_030938 6 BNO743 BCAT1 branched chain aminotransferase 1, cytosolic Hs.438993 NM_005504 0.5, 24   BNO744 PJA2 Praja 2, RING-H2 motif containing Hs.224262 NM_014819 BNO746 FKSG14 leucine zipper protein FKSG14 Hs.192843 NM_022145 6 BNO748 KLHL6 kelch-like 6 (Drosophila) Hs.43616 NM_130446 6 BNO749 TTL Tubulin tyrosine ligase Hs.358997 NM_153712 6 BNO750 CDC23 CDC23 (cell division cycle 23, yeast, homolog) Hs.153546 NM_004661 24  BNO751 ULK2 unc-51-like kinase 2 (C. elegans) Hs.151406 NM_014683 3 BNO752 SCARB2 SCARB2 Scavenger receptor class B, member 2 Hs.323567 NM_005506E 3 BNO755 ZMPSTE24 zinc metalloproteinase (STE24 homolog, yeast) Hs.25846 NM_005857 BNO757 U5-100K prp28, U5 snRNP 100 kd protein Hs.184771 NM_004818 BNO758 CHD4 chromodomain helicase DNA binding protein 4 Hs.74441 NM_001273 6 BNO760 CGI-127 yippee protein Hs.184542 NM_016061 3, 24 BNO763 BET1 BET1 homolog (S. cerevisiae) Hs.23103 NM_005868 24  BNO764 ARHGAP5 Rho GTPase activating protein 5 Hs.267831 NM_001173 BNO765 TUBA Scaffold protein TUBA Hs.429994 NM_015221 3 BNO766 NUMB numb homolog (Drosophila) Hs.78890 NM_003744 6 BNO767 P5 protein disulfide isomerase-related protein Hs.182429 NM_005742   0.5 BNO769 SFRS2IP splicing factor, arginine/serine-rich 2, interacting protein Hs.51957 NM_004719 6 BNO770 OXA1L oxidase (cytochrome c) assembly 1-like Hs.151134 NM_005015 0.5, 24   BNO771 POH1 26S proteasome-associated pad1 homolog Hs.178761 NM_005805 6 BNO773 AHCYL1 S-adenosylhomocysteine hydrolase-like 1 Hs.4113 NM_006621 3 BNO774 UAP1 UDP-N-acteylglucosamine pyrophosphorylase 1 Hs.21293 NM_003115 3 BNO775 PLS3 plastin 3 (T isoform) Hs.4114 NM_005032 6 BNO776 TSNAX translin-associated factor X Hs.96247 NM_005999   0.5 BNO777 HELO1 homolog of yeast long chain polyunsaturated fatty acid elong. enz. 2 Hs.250175 NM_021814 6 BNO778 MAN2A1 mannosidase, alpha, class 2A, member 1 Hs.377915 NM_002372 3 BNO779 RAB21 RAB21, member RAS oncogene family Hs.184627 NM_014999 6 BNO781 WAC WW domain-containing adapter with a coiled-coil region Hs.70333 NM_016628 3 BNO783 POSH likely ortholog of mouse plenty of SH3 domains Hs.301804 AB040927 6 BNO784 RBM9 RNA binding motif protein 9 Hs.433574 NM_014309 BNO785 CSRP2 cysteine and glycine-rich protein 2 Hs.10526 NM_001321 3 BNO786 COPA coatomer protein complex, subunit alpha Hs.75887 NM_004371 6 BNO787 TIMM17A translocase of inner mitochondrial membrane 17 homolog A (yeast) Hs.20716 NM_006335 6 BNO788 RIN2 Ras and Rab interactor 2 Hs.62349 NM_018993 24  BNO789 KLHL5 kelch-like 5 (Drosophila) Hs.272239 NM_015990 24  BNO790 IPLA2(γ) intracellular memb.-assoc. calcium-independent phospholipase A2γ Hs.44198 AF263613 6 BNO794 SMARCA5 SWI/SNF related regulator of chromatin, a5 Hs.9456 NM_003601 BNO796 FBXL3A F-box and leucine-rich repeat protein 3A Hs.7540 NM_012158 24  BNO797 SART2 squamous cell carcinoma antigen recognized by T cell Hs.58636 NM_013352E 6 BNO798 YWHAZ 14-3-3zeta Hs.386834 NM_145690 BNO799 SH3BGRL2 SH3 domain binding glutamic acid-rich protein like 2 Hs.9167 NM_031469 3, 24 BNO801 PUM1 pumilio homolog 1 (Drosophila) Hs.153834 NM_014676 3 BNO803 CCT2 chaperonin containing TCP1, subunit 2 (beta) Hs.432970 NM_006431 6 BNO804 PTPRK protein tyrosine phosphatase, receptor type, K Hs.79005 NM_002844 6 BNO806 TM4SF1 transmembrane 4 superfamily member 1 Hs.351316 NM_014220 6 BNO807 CHSY1 carbohydrate (chondroitin) synthase 1 Hs.110488 NM_014918 24  BNO808 TERF2IP telomeric repeat binding factor 2, interacting protein Hs.274428 NM_018975 6 BNO809 RDC1 G protein-coupled receptor Hs.23016 BC036661 3 BNO810 CD59 CD59 antigen p18-20 Hs.278573 AK095453 0.5, 6 BNO811 UBE2D1 ubiquitin-conjugating enzyme E2D 1 (UBC4/5 homolog, yeast) Hs.129683 NM_003338 6 BNO813 CUL4B cullin 4B Hs.155976 NM_003588 24  BNO814 LCHN LCHN protein Hs.233044 AB032973 3 BNO815 PELO pelota homolog (Drosophila) Hs.5798 NM_015946 3 BNO817 MRPS10 mitochondrial ribosomal protein S10 Hs.380887 NM_018141 6 BNO820 EIF3S2 eukaryotic translation initiation factor 3, subunit 2 beta, 36 kDa Hs.192023 NM_003757 3 BNO822 UBQLN1 ubiquilin 1 Hs.9589 NM_013438 3 BNO823 PSMB3 proteasome (prosome, macropain) subunit, beta type, 3 Hs.82793 NM_002795 0.5, 24   BNO826 UBE2J1 ubiquitin-conjugating enzyme E2, J1 (UBC6 homolog, yeast) Hs.184325 NM_016336 24  BNO827 CDK2AP1 CDK2-associated protein 1 Hs.433201 NM_004642 24  BNO828 CRY1 cryptochrome 1 (photolyase-like) Hs.151573 NM_004075 3 BNO830 HSPC051 ubiquinol-cytochrome c reductase complex (7.2 kD) Hs.284292 NM_013387 6 BNO832 GNG11 guanine nucleotide binding protein (G protein), gamma 11 Hs.83381 NM_004126 0.5, 24   BNO834 ZNF198 zinc finger protein 198 Hs.109526 NM_003453 6 BNO835 RAB11A RAB11A, member RAS oncogene family Hs.75618 NM_004663 6 BNO836 SMAP1 stromal membrane-associated protein Hs.373517 NM_021940 6 BNO837 COPG Coatomer protein complex, subunit gamma Hs.368056 NM_016128 3 BNO839 MTHFD2 methylene tetrahydrofolate dehydrogenase (NAD+ dependent) Hs.154672 NM_006636 3 BNO840 PODXL podocalyxin-like Hs.16426 NM_005397 6 BNO841 SLC30A7 Solute carrier family 30 (zinc transporter), member 7 Hs.38856 NM_133496 3 BNO842 API5 apoptosis inhibitor 5 Hs.227913 NM_006595 3 BNO843 ERdj5 ER-resident protein ERdj5 Hs.1098 NM_018981 3 BNO844 HDGFRP3 Hepatoma-derived growth factor, related protein 3 Hs.127842 NM_016073 6 BNO847 TUCAN tumor up-regulated CARD-containing antagonist of caspase nine Hs.10031 NM_014959 6 BNO850 PCDH17 protocadherin 17 Hs.106511 NM_014459 24  BNO851 GALNT10 N-acetylgalactosaminyltransferase 10 Hs.107260 NM_017540 24  BNO853 UQCRC1 ubiquinol-cytochrome c reductase core protein I Hs.119251 NM_003365 6 BNO854 RPL3 ribosomal protein L3 Hs.119598 NM_000967 24  BNO855 CMT2 gene predicted from cDNA with a complete coding sequence Hs.124 NM_014628 24  BNO858 PSMD7 proteasome 26S subunit, non-ATPase, 7 Hs.155543 NM_002811 6 BNO859 CCT5 chaperonin containing TCP1, subunit 5 (epsilon) Hs.1600 NM_012073 3 BNO860 SEC5 homolog of yeast Sec5 Hs.16580 NM_018303 6 BNO861 SKP1A S-phase kinase-associated protein 1A (p19A) Hs.171626 NM_006930 24  BNO863 CAPZA1 capping protein (actin filament) muscle Z-line, alpha 1 Hs.184270 NM_006135 24  BNO864 YES1 v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1 Hs.194148 NM_005433 24  BNO865 DAAM1 dishevelled associated activator of morphogenesis 1 Hs.197751 NM_014992 6 BNO866 BCL6B B-cell CLL/lymphoma 6, member B (zinc finger protein) Hs.22575 NM_181844 6 BNO872 AF5Q31 ALL1 fused gene from 5q31 Hs.231967 NM_014423 6 BNO874 ALDH9A1 aldehyde dehydrogenase 9 family, member A1 Hs.2533 NM_000696 24  BNO875 CDC42EP3 CDC42 effector protein (Rho GTPase binding) 3 Hs.260024 NM_006449 0.5, 24   BNO877 MIS12 homolog of yeast Mis12 Hs.267194 NM_024039 6 BNO879 ATP6V1D ATPase, H+ transporting, lysosomal 34 kDa, V1 subunit D Hs.272630 NM_015994 6 BNO880 VCIP135 valosin-containing protein (p97)/p47 complex-interacting protein p135 Hs.287727 NM_025054 6 BNO882 D10S170 DNA segment on chromosome 10 (unique) 170 Hs.288862 NM_005436 6 BNO884 ARPC3 actin related protein 2/3 complex, subunit 3, 21 kDa Hs.293750 NM_005719 24  BNO885 RPS19 ribosomal protein S19 Hs.298262 NM_001022 6 BNO888 NEUGRIN mesenchymal stem cell protein DSC92 Hs.323467 NM_016645 6 BNO889 CALD1 caldesmon 1 Hs.325474 NM_033138   0.5 BNO891 NFIB nuclear factor I/B Hs.33287 NM_005596   0.5 BNO893 HSPCA heat shock 90 kDa protein 1, alpha Hs.356531 NM_005348 6 BNO896 NSAP1 NS1-associated protein 1 Hs.373499 NM_006372 6 BNO897 SYT11 synaptotagmin XI Hs.380439 NM_152280 6 BNO899 HNRPC heterogeneous nuclear ribonucleoprotein C (C1/C2) Hs.406125 NM_006321 24  BNO900 STMN1 stathmin 1/oncoprotein 18 Hs.406269 NM_005563 6 BNO901 ATP5B ATP synthase, H+ transporting, mitochondrial F1 complex, beta Hs.406510 NM_001686 0.5, 24   BNO902 PSMB1 proteasome (prosome, macropain) subunit, beta type, 1 Hs.407981 NM_002793 0.5, 24   BNO903 DDX10 DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 10 (RNA helicase) Hs.41706 NM_004398 6 BNO904 RPL36AL ribosomal protein L36a-like Hs.419465 NM_001001 24  BNO907 NDUFV2 NADH dehydrogenase (ubiquinone) flavoprotein 2, 24 kDa Hs.51299 NM_021074 0.5, 24   BNO909 DCK deoxycytidine kinase Hs.709 NM_000788 24  BNO911 MDH1 malate dehydrogenase 1, NAD (soluble) Hs.75375 NM_005917 24  BNO912 SERP1 stress-associated endoplasmic reticulum protein 1 Hs.76698 NM_014445   0.5 BNO913 RPS3A ribosomal protein S3A Hs.77039 NM_001006   0.5 BNO914 ARHA ras homolog gene family, member A Hs.77273 NM_001664   0.5 BNO915 LAMA4 laminin, alpha 4 Hs.78672 NM_002290 6 BNO916 SNX9 sorting nexin 9 Hs.7905 NM_016224 6 BNO918 RAD21 RAD21 homolog (S. pombe) Hs.81848 NM_006265 0.5, 24   BNO920 PHLDA1 pleckstrin homology-like domain, family A, member 1 Hs.82101 NM_007350 6 BNO921 ARHGDIB Rho GDP dissociation inhibitor (GDI) beta Hs.83656 NM_001175 24  BNO922 ELP2 elongator protein 2 Hs.8739 NM_018255 6 BNO924 ATP6V1G1 ATPase, H+ transporting, lysosomal 13 kDa, V1 subunit G isoform 1 Hs.90336 NM_004888 24  BNO925 DNAJA1 DnaJ (Hsp40) homolog, subfamily A, member 1 Hs.94 NM_001539 3 BNO927 CYB561 cytochrome b-561 None NM_001915 24  BNO947 HNRPDL Heterogeneous nuclear ribonucleoprotein D-like Hs.372673 NM_005463 3 BNO952 ARHB Ras homolog gene family, member B Hs.406064 NM_004040 3 BNO955 CYB561 Cytochrome b-561 Hs.355264 AK095244 24  BNO958 ATP6 ATP synthase F0 subunit 6 - mitochondrial gene None NC_001807 24  BNO969 ND4L NADH dehydrogenase subunit 4L - mitochondrial gene None NC_001807 6 BNO960 COX2 cytochrome C oxidase subunit II - mitochondrial gene None NC_001807 0.5, 24   BNO1014 SET SET translocation (myeloid leukemia-associated) Hs.145279 NM_003011 6 BNO1015 JUNB jun B proto-oncogene Hs.400124 NM_002229   0.5 BNO1016 HMGB1 high-mobility group box 1 Hs.6727 NM_002128 6 BNO1017 PAFAH1B2 Platelet-activating factor acetylhydrolase, isoform Ib, beta subunit Hs.93354 NM_002572 24 

TABLE 3 Genes Previously Associated with Angiogenesis BNO UniGene GenBank Peak Number Symbol Gene Description - Homology Number Number Expression (h) BNO435 ICAM1 intercellular adhesion molecule 1 (CD54), human rhinovirus Hs.168383 NM_000201 3 receptor BNO437 IL8 interleukin 8 Hs.624 NM_000584 3 BNO439 VCAM1 vascular cell adhesion molecule 1 Hs.109225 NM_001078 3 BNO440 ANGPT2 angiopoietin 2 Hs.115181 NM_001147 6 BNO444 CTNNB1 catenin (cadherin-associated protein), beta 1, 88 kDa Hs.171271 NM_001904 3 BNO445 F3 coagulation factor III (thromboplastin, tissue factor) Hs.62192 NM_001993 3 BNO450 STC1 stanniocalcin 1 Hs.25590 NM_003155 24 BNO458 ADAMTS4 a disintegrin-like and metalloprotease (thrombospondin type 1 Hs.211604 NM_005099 6 motif, 4) BNO471 ESM1 endothelial cell-specific molecule 1 Hs.41716 NM_007036 3, 24 BNO482 CMG2 capillary morphogenesis protein 2 Hs.5897 NM_058172 6 BNO486 EFNB2 ephrin-B2 Hs.30942 NM_004093 3 BNO493 PTGS1 prostaglandin-endoperoxide synthase 1 Hs.88474 NM_000962 6 BNO494 KDR kinase insert domain receptor (a type III receptor tyrosine kinase) Hs.12337 NM_002253 BNO522 F2R coagulation factor II (thrombin) receptor Hs.128087 NM_001992 3 BNO529 CTSB cathepsin B Hs.297939 NM_001908 24 BNO530 LIF leukemia inhibitory factor (cholinergic differentiation factor) Hs.2250 NM_002309 3 BNO547 EDN1 endothelin 1 Hs.2271 NM_001955E 0.5 BNO550 JAK1 Janus kinase 1 (a protein tyrosine kinase) Hs.50651 NM_002227 24 BNO563 THBD thrombomodulin Hs.2030 NM_000361 24 BNO592 PSEN1 presenilin 1 (Alzheimer disease 3) Hs.3260 NM_000021 0.5 BNO593 STAT3 signal transducer and activator of transcription 3 Hs.321677 NM_139276 6 BNO601 GJA1 gap junction protein, alpha 1, 43 kDa (connexin 43) Hs.74471 NM_000165 3 BNO608 HEY1 hairy/enhancer-of-split related with YRPW motif 1 Hs.234434 NM_012258 0.5 BNO846 CXCR4 chemokine (C—X—C motif) receptor 4 Hs.89414 NM_003467 24 BNO869 ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1 Hs.205353 NM_001776 0.5 BNO919 SERPINE1 serine (or cysteine) proteinase inhibitor, clade E, member 1 Hs.82085 NM_000602 3 BNO923 THBS1 thrombospondin 1 Hs.87409 NM_003246 0.5

REFERENCES

References cited herein are listed on the following pages, and are incorporated herein by this reference.

-   Altschul, S F. et al. (1997). Nucleic Acids Res. 25: 3389-3402. -   Breaker, R R. and Joyce, GF. (1995). Chem. Biol. 2: 655-600. -   Cole, S P. et al. (1984). Mol. Cell Biol. 62: 109-120. -   Cote, R J. et al. (1983). Proc. Natl. Acad. Sci. USA 80: 2026-2030. -   Culver, K. (1996). Gene Therapy: A Primer for Physicians. Second     Edition. (Mary Ann Liebert). -   Folkman, J. and Haudenschild, C. (1980). Nature (Lond.) 288:     551-556. -   Friedman, T. (1991). In Therapy for Genetic Diseases. (T Friedman     (Ed) Oxford University Press. pp 105-121. -   Gamble, J R. et al. (1993). J. Cell Biol. 121: 931-943. -   Gamble, J R. et al. (1999). Endothelium 7: 23-34. -   Gecz, J. et al. (1997). Genomics 44: 201-213. -   Goldman, C K. et al. (1997). Nature Biotechnology 15: 462-466. -   Green, L L. et al. (1994). Nature Genet. 7: 13-21. -   Grishok, A. et al. (2001). Science 287: 2494-2497. -   Haseloff, J. and Gerlach, W L. (1988). Nature 334: 585-591. -   Heller, R A. et al. (1997). Proc. Natl. Acad. Sci. USA 94:     2150-2155. -   Huse, W D. et al. (1989). Science 246: 1275-1281. -   Kohler, G. and Milstein, C. (1975). Nature 256: 495-497. -   Kozbor, D. et al. (1985). J. Immunol. Methods 81:31-42. -   Lonberg, N. et al. (1994). Nature 368: 856-859. -   Meyer, G T. et al. (1997). The Anatomical Record 249: 327-340. -   Orlandi, R. et al. (1989). Proc. Natl. Acad. Sci. USA 86: 3833-3837. -   Rickert, R C. et al. (1997). Nucleic Acids Res. 25: 1317-1318. -   Sambrook, J. et al. (1989). Molecular cloning: a laboratory manual.     Second Edition. (Cold Spring Harbour Laboratory Press, New York). -   Scharf, D. et al. (1994). Results Probl. Cell Differ. 20: 125-162. -   Schena, M. et al. (1996). Proc. Natl. Acad. Sci. USA 93:     10614-10619. -   Schwenk, F. et al. (1995). Nucleic Acids Res. 23: 5080-5081. -   Sharp, P A. and Zamore, P D. (2000). Science 287: 2431-2432. -   Taylor, L D. et al. (1994). Int. Immunol. 6: 579-591. -   Winter, G. et al. (1991). Nature 349: 293-299. 

1. A method for the identification of a nucleic acid molecule differentially expressed in an in vitro model of a biological system, comprising the steps of: (1) harvesting cells from the model system at predetermined time points; (2) obtaining total RNA from the cells harvested at each time point; (3) preparing cDNA from the total RNA from each time point to provide a plurality of pools of cDNA; (4) performing a suppression subtractive hybridization (SSH) on the cDNA pools from each time point sequentially so as to progressively amplify cDNAs derived from nucleic acid molecules differentially expressed from one time period to the next.
 2. A method as claimed in claim 1 wherein the model system is an in vitro model for angiogenesis.
 3. A nucleic acid molecule differentially expressed during angiogenesis when identified by the method of claim 1 or claim
 2. 4. A nucleic acid molecule as claimed in claim 3 selected from the group consisting of those laid out in Tables 1 and
 2. 5. A method for the identification of a nucleic acid molecule up-regulated in an in vitro model of a biological system, comprising the steps of: (1) harvesting cells from the model system at predetermined time points; (2) obtaining total RNA from the cells harvested at each time point; (3) preparing cDNA from the total RNA from each time point to provide a plurality of pools of cDNA; (4) performing a suppression subtractive hybridization (SSH) on the cDNA pools from each time point sequentially so as to progressively amplify cDNAs derived from nucleic acid molecules differentially expressed from one time period to the next. (5) cloning the amplified cDNAs; (6) locating DNA from each clone on a microarray; (7) generating antisense RNA by reverse transcription of total RNA from cells harvested from the in vitro model at said predetermined time intervals and labelling the antisense RNA; and (8) probing the microarray with labelled antisense RNA from 0 hours and each of the other time points separately to identify clones containing cDNA derived from nucleic acid molecules which are up-regulated at said time points in the in vitro model.
 6. A method as claimed in claim 5 wherein the in vitro model is an in vitro model for angiogenesis.
 7. A nucleic acid molecule when identified by the method of claim 5 or claim
 6. 8. A nucleic acid molecule as claimed in claim 7 selected from the group consisting of those set forth in Tables 1 and
 2. 9. A polypeptide encoded by a nucleic acid molecule as claimed in any one of claims 3, 4, 7 or
 8. 10. An isolated nucleic acid molecule comprising the sequence set forth in one of SEQ ID Numbers: 1 to
 44. 11. An isolated nucleic acid molecule comprising the sequence set forth in one of SEQ ID Numbers: 1 to 44 or as laid out in Tables 1 and 2, or a fragment thereof, and which encodes a polypeptide that plays a role in an angiogenic process.
 12. An isolated nucleic acid molecule that is at least 70% identical to a nucleic acid molecule comprising the sequence set forth in one of SEQ ID Numbers: 1 to 44 or as laid out in Tables 1 and 2, and which encodes a polypeptide that plays a role in an angiogenic process.
 13. An isolated nucleic acid molecule as claimed in claim 12 that is at least 85% identical.
 14. An isolated nucleic acid molecule as claimed in claim 12 that is at least 95% identical.
 15. An isolated nucleic acid molecule that encodes a polypeptide that plays a role in an angiogenic process, and which hybridizes under stringent conditions with a nucleic acid molecule comprising the nucleotide sequence set forth in one of SEQ ID Numbers: 1 to 44 or as laid out in Tables 1 and
 2. 16. An isolated nucleic acid molecule as claimed in any one of claims 10 to 15, which encodes a polypeptide that plays a role in diseases associated with angiogenesis including but not restricted to cancer, rheumatoid arthritis, diabetic retinopathy, psoriasis, cardiovascular diseases such as atherosclerosis, ischaemic limb disease and coronary artery disease.
 17. An isolated nucleic acid molecule consisting any one of the nucleotide sequences set forth in SEQ ID Numbers: 1 to
 44. 18. Use of a nucleic acid molecule selected from the group consisting of DNA molecules having the sequence set forth in SEQ ID Numbers: 1 to 15, 17 to 37, and 39 to 44 to identify and/or obtain full-length human genes involved in an angiogenic process.
 19. Use as claimed in claim 18 wherein additional sequence is obtained using hybridization with one or more of said nucleic acid molecules, inverse PCR, restriction site PCR, PCR walking techniques or RACE.
 20. A gene when identified by the use of a nucleic acid molecule selected from any one of SEQ ID Numbers: 1 to 15, 17 to 37, and 39 to 44
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 28. An expression vector comprising a nucleic acid molecule as claimed in any one of claims 3 to 4, claims 7 to 8, or claims 10 to
 17. 29. A cell comprising an expression vector of claim
 28. 30. A cell as claimed in claim 29 which is an eukaryotic cell.
 31. A method of preparing a polypeptide comprising the steps of: (1) culturing cells as claimed in either one of claims 29 or 30 under conditions effective for polypeptide production; and (2) harvesting the polypeptide.
 32. A polypeptide prepared by the method of claim
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 112. A short interfering oligonucleotide targeted to the mRNA encoded by a nucleic acid molecule as claimed in claim
 10. 113. A catalytic nucleic acid molecule targeted to a nucleic acid molecule as claimed in claim
 10. 114. A catalytic nucleic acid molecule of claim 113 which is a DNAzyme.
 115. A catalytic nucleic acid molecule of claim 113 which is a ribozyme.
 116. Use of a nucleic acid molecule as claimed in any one of claims 3 to 4, claims 7 to 8, or claims 10 to 17 in the diagnosis or prognosis of an angiogenesis-related disorder.
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 128. A genetically modified non-human animal comprising a isolated a nucleic acid molecule as claimed in any one of claims 3 to 4, claims 7 to 8, or claims 10 to
 17. 129. A genetically modified non-human animal comprising a disruption of a nucleic acid molecule as claimed in any one of claims 3 to 4, claims 7 to 8, or claims 10 to
 17. 130. A genetically modified non-human animal as claimed in either one of claims 128 or 129 in which the animal is selected from the group consisting of rats, mice, hamsters, guinea pigs, rabbits, dogs, cats, goats, sheep, pigs and non-human primates such as monkeys and chimpanzees.
 131. A genetically modified non-human animal as claimed in any one of claims 128 to 130 wherein the animal is a mouse.
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